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Class Number: 560 Class Title: ORGANIC COMPOUNDS -- PART OF THE CLASS 532-570 SERIES Subclass Subclass Number Title * ORGANIC COMPOUNDS (Class 532, Subclass 1) 1 .Carboxylic acid esters 2 ..With preservative 3 ...Aromatic polycarboxylic acid esters 4 ...Acyclic unsaturated monocarboxylic acid esters 5 ..Hydrophenanthrene in acid moiety 6 ...Polycyclo ring system having the hydrophenanthrene and at least one additional ring as cyclos 7 ...1,4a-Dimethylhydrophenanthrene-1- carboxylic acid 8 ..Aromatic acid moiety 9 ...Sulfur in acid moiety 10 ....Ortho fused rings in acid moiety 11 ....Sulfoxy in acid moiety 12 .....Nitrogen in acid moiety 13 ......Plural nitrogens in acid moiety 14 .....Sulfonic acids, salts or acid halides 15 ....Sulfur, not bonded directly to a ring, in same side chain as ester function 16 .....Nitrogen in acid moiety 17 ....Sulfur, bonded directly to a ring, in same side chain as ester function 18 ....Ester function attached directly to a ring 19 ...Nitrogen in acid moiety other than as nitroso or isocyanate (e.g., amino acid esters, etc.) 20 ....Nitro bonded to carbon in acid moiety 21 .....Plural rings in acid moiety 22 .....Additional nitrogen in acid moiety 23 .....Oxy, aldehyde or ketone group in acid moiety 24 ....Carbamic acid 25 .....Polycarbamic 26 ......Polyoxy alcohol moiety 27 .....Plural rings in acid moiety 28 ......Ortho fused 29 .....Oxy in acid moiety 30 .....Halogen in acid moiety 31 ......Ring in alcohol moiety 32 .....Ring in alcohol moiety 33 .....Sulfur, nitrogen, halogen or additional oxy in alcohol moiety 34 ....Ureido, guanido or hydrazino in acid moiety 35 ....Amidine, azomethine, ketimine or oxime in acid moiety 36 ....Plural rings bonded directly to the same cyclic carbon in acid moiety 37 ....The nitrogen is not bonded directly to a ring 38 .....The nitrogen is in same side chain as ester function 39 ......Oxy in acid moiety 40 .......Phenylalanines 41 ......Amide in acid moiety 42 .....Oxy in acid moiety 43 ....The nitrogen is bonded directly to a ring and is in same side chain as ester function 44 .....Polycarboxylic acidd 45 ....Oxy in acid moiety 46 .....Benzoic acid substituted on ring with oxy and nitrogen 47 ....Halogen in acid moiety 48 ....Plural rings in acid moiety with nitrogen bonded directly to at least one of the rings 49 ....Nitrogen in alcohol moiety 50 ....Polyoxy alcohol moiety 51 ...Aldehyde or ketone group in acid moiety 52 ....Plural rings bonded directly to the same carbonyl in acid moiety 53 ....Oxy in acid moiety 54 ....Polycarboxylic acid 55 ...Oxy in acid moiety 56 ....Ortho fused rings in acid moiety 57 ....Plural rings bonded directly to the same acyclic carbon in acid moiety 58 .....Nitrogen in alcohol moiety 59 ....Rings bonded directly to each other in acid moiety 60 ....Oxy, not bonded directly to a ring, in same side chain as ester function 61 ....Oxy, bonded directly to a ring, in same side chain as ester function 62 .....Halogen in acid moiety 63 ......Polyoxy alcohol moiety 64 ....Ester function attached directly to a ring 65 .....Halogen in acid moiety 66 .....Acylated 67 .....Phenolic hydroxy or metallate 68 ......Tannins and reaction products thereof 69 .......Extraction from bark or vegetable material 70 ......Polyphenolic hydroxy or metallate 71 ......Salicylic acid 72 ......Ring in alcohol moiety 73 .....Ring in alcohol moiety 74 .....Nitrogen in alcohol moiety 75 ....Phenolic hydroxy or metallate 76 ...Polycarboxylic acid 77 ....Producing carboxyl group by oxidation 78 ....Purification or recovery 79 .....Of ester of polyoxy alcohols 80 ....Ortho fused rings in acid moiety 81 ....Esterified carboxy not bonded directly to a ring 82 .....Malonates 83 ....Halogen in acid moiety 84 ....Ring in alcohol moiety 85 .....Aromatic alcohol moiety 86 ......Esterified phenolic hydroxy 87 ....Sulfur or halogen in alcohol moiety 88 ....Nitrogen in alcohol moiety 89 ....Polyoxy alcohol moiety 90 .....Additional esterifying acid 91 .....Polyoxyalkylene alcohol moiety 92 .....Preparing esters by ester interchange 93 .....Preparing esters from alkylene oxides 94 .....Preparing esters from acid or from nitrile and diol 95 ....Unsaturation in alcohol moiety 96 ....Processes 97 .....Carbonylationn 98 .....Esterification of acid, salt, acid halide or anhydride with alcohol 99 ......Metal containing catalyst utilized 100 ...Naphthyl in acid moiety 101 ...Plural rings bonded directly to the same carbon in acid moiety 102 ...Rings bonded directly to each other in acid moiety 103 ...Monocyclic acid moiety 104 ....Additional unsaturation in acid moiety 105 ....Carboxyl, not bonded directly to a ring, in acid moiety 106 ....Ring in alcohol moiety 107 .....Plural rings in alcohol moiety 108 ......Esterified phenolic hydroxy 109 .....Esterified phenolic hydroxy 110 ....Nitrogen in alcohol moiety 111 ....Halogen in alcohol moiety 112 ....Polyoxy alcohol moiety 113 ....Unsaturation in alcohol moiety 114 ..Preparing alicyclic acid esters by carbonylation 115 ..Alicyclic carbamates 116 ..Plural alicyclic rings in acid moiety 117 ...Tricyclo ring system in acid moiety 118 ...Two rings only in acid moiety 119 ....Ortho fused 120 ....2,2,1-bicyclo 121 ..Cyclopentyl in acid moiety (e.g., prostaglandins, etc.) 122 ...Cyclopentyl-COOR, -C-COOR or -C-C-COOR 123 ..Cyclobutyl in acid moiety 124 ..Cyclopropyl in acid moiety 125 ..Alicyclic acid moiety containing N, S, P, B or halogen 126 ..Alicyclic acid moiety containing oxy, aldehyde or ketone group 127 ..Alicyclic polycarboxylic acid moiety 128 ..Alicyclic acid moiety containing unsaturation 129 ..Acyclic acid moiety 130 ...Esterified phenolic hydroxy 131 ....Preparing esters by oxidation 132 ....Carbamic acid 133 .....Plural rings in phenolic moiety 134 ......Ortho fused 135 .....Sulfur in phenolic moiety 136 .....Nitrogen in phenolic moiety 137 .....Sulfur, halogen or additional nitrogen or oxygen in carbamic acid moiety 138 ....Plural rings in phenolic moiety 139 .....Ortho fused 140 .....Plural rings bonded directly to the same carbon in phenolic moiety 141 .....Rings bonded directly to each other in phenolic moiety 142 ....Nitrogen or sulfur in phenolic moiety 143 ....Salicylic acid or functional derivative 144 ....Polyoxy phenolic moiety 145 ....Sulfur, nitrogen, halogen, oxy, or aldehyde or ketone group in acid moiety 146 ....Polycarboxylic acid 147 ...Sulfur in acid moiety 148 ....Carbamic acid 149 ....Sulfoxy in acid moietyy 150 .....Sulfonyl or sulfinyl in acid moiety 151 .....Polycarboxylic acid 152 ....Thio ether in acid moiety 153 .....Nitrogen or halogen in acid moiety 154 .....Polycarboxylic acid 155 ...Nitrogen in acid moiety other than as nitroso or isocyanate (e.g., amino acid esters, etc.) 156 ....Nitro bonded to carbon in acid moiety 157 ....Carbamic acid 158 .....Polycarbamic 159 .....Additional nitrogen in acid moiety 160 .....Oxy in acid moiety 161 .....Halogen in acid moiety 162 .....Cyclic alcohol moiety 163 ......Aromatic alcohol moiety 164 .......Polyoxy alcohol moiety 165 .....Sulfur or nitrogen in alcohol moiety 166 .....Polyoxy alcohol moiety 167 .....Halogen in alcohol moiety 168 ....Amidine, azomethine, ketimine or oxime in acid moiety 169 ....Additional nitrogen in acid moiety 170 ....Oxy, aldehyde or ketone group in acid moiety 171 ....Polycarboxylic acid 172 ....Halogen or unsaturation in acid moiety 173 ....Cyclic alcohol moiety 174 ...Aldehyde or ketone group in acid moiety 175 ....Preparing esters by carbonylation 176 ....Polycarboxylic acid 177 ....Aldehyde group in acid moiety 178 ....Acetoacetic acid 179 ...Oxy in acid moiety 180 ....Polycarboxylic acid 181 .....Unsaturation in acid moiety 182 .....Polyoxy alcohol moiety 183 ....Unsaturation in acid moiety 184 ....Halogen in acid moiety 185 ....Acylated oxy in acid moiety 186 ....Polyoxy acid moiety 187 ....Alkoxy in acid moiety 188 ....Cyclic alcohol moiety 189 ....Polyoxy alcohol moiety 190 ...Polycarboxylic acid 191 ....Purification or recovery 192 ....Halogen in acid moiety 193 ....Cyclic alcohol moiety 194 .....Plural rings in alcohol moiety 195 ....Phosphorus or sulfur in alcohol moiety 196 ....Nitrogen in alcohol moiety 197 ....Halogen in alcohol moiety 198 ....Polyoxy alcohol moiety 199 .....Additional monooxy alcohol or monocarboxylic acid (e.g., complex esters, etc.) 200 .....Preparing esters from alkylene oxides 201 ....Unsaturation in alcohol moiety 202 ....Preparing esters by oligomerization 203 ....Preparing esters by alkylation or isomerization 204 ....Preparing esters by esterification or carbonylation 205 ...Unsaturation in acid moietyy 206 ....Preparing esters by carbonylation 207 .....Group VIII noble metal catalyst utilized 208 ....Formation of carboxyl group by oxidation 209 ....Preparing esters from alkylene oxides 210 ....Preparing esters from aldehydes 211 ....Formation of ethylenic unsaturation 212 .....By dehydration or dealcoholization 213 .....By dehalogenation or dehydrohalogenation 214 .....By dehydrogenation 215 ....Preparing esters from nitriles or amides 216 ....Preparing esters by depolymerization 217 ....Preparing esters by ester interchange 218 ....Purification or recovery 219 ....Halogen in acid moiety 220 ....Cyclic alcohol moiety 221 .....Aromatic alcohol moiety 222 ....Phosphorus, sulfur or nitrogen in alcohol moiety 223 ....Halogen in alcohol moiety 224 ....Polyoxy alcohol moiety 225 ....Unsaturation in alcohol moiety 226 ...Halogen in acid moiety 227 ....Fluorine in acid moiety 228 ....Cyclic alcohol moiety 229 ....Halogen in alcohol moiety 230 ....Polyoxy alcohol moiety 231 ...Unsubstituted acids of the acetic series 232 ....Preparing esters by carbonylation 233 .....Of olefins 234 ....Preparing esters by ester interchange 235 .....From alkyl sulfates 236 ....Preparing esters from halogenated hydrocarbons 237 .....From alkenyl halides 238 ....Preparing esters from aldehydes 239 ....Preparing esters by dehydrogenation of alcohols 240 ....Preparing esters from ethers 241 ....Preparing esters from hydrocarbons 241.1 .....By oxidation of hydrocarbon mixtures 242 .....From acetylenic hydrocarbons 243 .....From olefins utilizing Group VIII noble metal catalyst 244 ......From polyolefins 245 ......Gas phase 246 .....Preparing polyoxy alcohol esters from olefins 247 .....Preparing alkyl esters from olefins 248 ....Purification or recovery 249 ....Terpene alcohol moiety 250 ....Nitrogen in alcohol moiety other than as nitro, nitroso or isocyanate 251 .....Plural nitrogens in alcohol moiety 252 .....Polyoxy alcohol moiety 253 .....Acyclic alcohol moiety 254 ....Aromatic alcohol moiety 255 .....Plural rings in alcohol moiety 256 ....Polycyclo-alicyclic ring system in alcohol moiety 257 .....Nor- or homo- cyclopentanohydrophenanthrenes 258 ......Nor-A ring 259 ....2,6,6-trialkyl cyclohexenyl in alcohol moiety 260 .....Vitamin A alcohol moiety 261 ....Acyclic alcohol moiety having unsaturationn 262 .....Substituted 263 ....Acyclic polyoxy alcohol moiety 264 .....Substituted 265 ....Acyclic monohydric alcohol moiety 266 .....Substituted 300 .Hypohalite or perhypohalite esters (i.e., compounds having the -O-halo group or the -O-O-halo group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 301 .Cyanate esters (i.e., compounds having the -OCN group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 302 .Compounds having the group -C(=X)-X-nX-, wherein the X's may be the same or diverse chalcogens, nX is a divalent chalcogen or a chain of divalent chalcogens single bonded to each other, and the terminal X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., percarboxylate esters, etc.) 303 .Sulfohydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -S(=O)(=O)-NH-X- group, wherein X is chalcogen and substitution may be made for hydrogen only, and wherein the X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 304 .Peroxynitrate esters (i.e., compounds having the -O-O-N(=O)(=O) group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 305 .Perborate esters or chalcogen analogues thereof (i.e., compounds having the -X-X- group, wherein the X's are the same or diverse chalcogens, bonded directly to boron and to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 306 .Perhalate esters (i.e., compounds having the -O-halo(=O)(=O)(=O) group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 307 .Esters having the -S(=O)(=O)-S- group, wherein the divalent sulfur is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., thiolsulfonate esters, etc.) 308 ..Oxygen bonded directly to the hexavalent sulfur of the -S(=O)(=O)-S- group (i.e., thiosulfate esters) 309 ...Nitrogen attached indirectly to the -S(=O)(=O)-S- group by acyclic nonionic bonding 310 .Esters having the -S(=O)-S- group, wherein the divalent sulfur is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (e.g., thiolsulfinate esters, dithiosulfurous acid esters, etc.) 311 .Perhydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -C(=X)-NH-X-X- group, wherein the X's are the same or diverse chalcogens and substitution may be made for hydrogen only, and wherein the terminal X is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 312 .Hydroxamate esters or chalcogen analogues thereof (i.e., compounds having the -C(=X)-NH-X- group, wherein the X's may be the same or diverse chalcogens and substitution may be made for hydrogen only, and wherein the single bonded X is bondedd directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 313 ..Nitrogen bonded directly to the carbon of the -C(=X)-NH-X- group 314 ...The single bonded X is sulfur, or the substituent nitrogen is bonded directly to acyclic or alicyclic carbon 315 ..Carbocyclic ring bonded directly to the carbon of the -C(=X)-NH-X- group 316 .Hyponitrite esters (i.e., compounds having the -O-N=N-O- group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 317 .Esters having the -N=S=O group bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon (i.e., sulfinylamines) 318 .Persulfonate esters (i.e., compounds having the -S(=O)(=O)-O-O- group, wherein the terminal oxygen is bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 319 .Perthioimidate esters (i.e., compounds having the perthioimidate group, HN=CH-S-S-, wherein substitution may be made for hydrogen only, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 330 .Isocyanate esters (i.e., compounds containing the isocyanate group, -N=C=O, bonded directly to carbon, which carbon may be single bonded to any atom but may be multiple bonded only to carbon) 331 ..With preservative or stabilizer 332 ...Nitrogen containing preservative or stabilizer 333 ...Phosphorus, silicon, or phenolic hydroxy containing preservative or stabilizer 334 ..Carbodiimide containing (i.e., -N=C=N- containing) 335 ..Biuret containing (i.e., -NH-C(=O)-NH-C(=O)-NH- containing, wherein substitution may be made for hydrogen only) 336 ..Processes 337 ...Isocyanic acid, or salt thereof, as reactant 338 ...Processes for forming the isocyanate group 339 ....Cyanate reactant (i.e., reactant contains -OCN group) 340 ....Hetero ring containing reactant 341 ....Carbon monoxide utilized 342 .....Reactant contains nitro group bonded directly to carbon 343 ....Azide reactant (i.e., reactant contains the azide group) 344 ....Reactant containing -NH-C(=O)-NH- group (wherein substitution may be made for hydrogen only) 345 ....Carbamate reactant (i.e., reactant contains -O-C(=O)-NH- group (wherein substitution may be made for hydrogen only) 346 ....Reactant containing nitrogen double or triple bonded to carbon (e.g., nitriles, isonitriles, cyanogen halides, etc.) 347 ....Carbonyl dihalide reactant (e.g., phosgene, etc.) 348 ....Carbamyl halide reactant (i.e., reactant contains halo-C(=O)-NH- group, wherein substitutuion may be made for hydrogen only) 349 ...Halogenation of isocyanate esters 350 ...Isocyanate exchange reactions (i.e., A-NCO + B-X = B-NCO + A-X) 351 ...Processes of reacting isocyanate esters of known structure to yield products of indeterminate structuree 352 ...Purification or recovery 353 ....Epoxy compound, or metal, utilized 354 ..Containing polycyclo ring system having alicyclic ring as one of the cyclos 355 ..Acyclic carbon bonded directly to the isocyanate group 356 ...Halogen attached indirectly to the isocyanate group by acyclic nonionic bonding 357 ...Chalcogen, single bonded directly to carbon, attached indirectly to the isocyanate group by acyclic nonionic bonding (e.g., ether group containing, etc.) 358 ..Benzene ring bonded directly to the isocyanate group 359 ...Plural benzene rings bonded directly to isocyanate groups (e.g., diisocyanatodiphenylmethane, etc.) 360 ...Plural isocyanate groups bonded directly to the same benzene ring