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HomeCarbamic acid derivatives / Carbamates / Carbamoyl chlorides / Thiocarbamoyl chlorides

Carbamic acid derivatives / Carbamates / Carbamoyl chlorides / Thiocarbamoyl chlorides


It is a class of compounds with amino carboxylic (or amino thiocarboxylic) functional group. Carbamic acids are generally unstable at room temperature, reverting to the parent amine and carbon dioxide. Carbamate esters are generally stable at room temperature. They are prepared by reaction of carbamoyl chlorides with alcohols, the addition of alcohols to isocyanates, and the reaction of carbonate esters with ammonia. Carbamate esters often serve as a protecting group for amines, which can be later hydrolyse to carbamic acid that lose carbon dioxide to yield desired amine.

Product nameStructureCAS#G-code
N,N-Bis-Boc-N-allylamineStructure of N,N-Bis-Boc-N-allylamine[115269-99-3]GEO-00330
1,6-Bis-Boc-1,6,10-triazadecaneStructure of 1,6-Bis-Boc-1,6,10-triazadecane[68076-39-1]GEO-04192
Boc-L-beta-HomoalanineStructure of Boc-L-beta-Homoalanine[158851-30-0]GEO-02625
Newtert-Butyl (S)-4-((R,E)-1-((tert-butyldimethylsilyl)oxy)hexadec-2-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylateStructure of tert-Butyl (S)-4-((R,E)-1-((tert-butyldimethylsilyl)oxy)hexadec-2-en-1-yl)-2,2-dimethyloxazolidine-3-carboxylate[]GEO-04610
Newtert-Butyl (4S)-4-[(1S,2E)-1-hydroxy-2-hexadecenyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylateStructure of tert-Butyl (4S)-4-[(1S,2E)-1-hydroxy-2-hexadecenyl]-2,2-dimethyl-1,3-oxazolidine-3-carboxylate[115464-04-5]GEO-04609
Chloroacetyl isocyanateStructure of Chloroacetyl isocyanate[4461-30-7]GEO-02756
N-Cyanoacetylurethane[6629-04-5]GEO-00827
N,N-DichlorourethaneStructure of N,N-Dichlorourethane[13698-16-3]GEO-01013
Diethylthiocarbamoyl chloride[88-11-9]GEO-03231
N-Boc-2,5-dihydro-1H-pyrroleStructure of N-Boc-2,5-dihydro-1H-pyrrole[73286-70-1]GEO-00377
4,6-Dihydro-1H,3H-thieno[3,4-c]furan-1,3-dione[75532-25-1]GEO-04022
N,N-Dimethylcarbamothioyl chlorideStructure of N,N-Dimethylcarbamothioyl chloride[16420-13-6]GEO-03077
Ethoxycarbonyl isocyanate[19617-43-7]GEO-01300
Ethyl allophanate[626-36-8]GEO-01310
Ethyl 2-chloroethylcarbamateStructure of Ethyl 2-chloroethylcarbamate[6329-26-6]GEO-01327
N-Methyl-N-phenylcarbamoyl chlorideStructure of N-Methyl-N-phenylcarbamoyl chloride[4285-42-1]GEO-03721
New1-Piperidinecarbonyl chlorideStructure of 1-Piperidinecarbonyl chloride[13939-69-0]GEO-03410
N-Boc-pyrrolidineStructure of N-Boc-pyrrolidine[86953-79-9]GEO-00379
1-Pyrrolidinecarbonyl chlorideStructure of 1-Pyrrolidinecarbonyl chloride[1192-63-8]GEO-03780
2,2,5,5-Tetramethyl-3-pyrrolidine-1-oxyl-3-carboxylic acid N-hydroxysuccinimide esterStructure of 2,2,5,5-Tetramethyl-3-pyrrolidine-1-oxyl-3-carboxylic acid N-hydroxysuccinimide ester[58537-73-8]GEO-02742
ThiophosgeneStructure of Thiophosgene[463-71-8]GEO-02306