Identification | Back Directory | [Name]
1-BOC-1,8-DIAMINOOCTANE | [CAS]
88829-82-7 | [Synonyms]
SKL028 Boc-DAOct 1-Boc-1,8-diaminooctan 1-BOC-1,8-DIAMINOOCTANE N1-BOC-1,8-DIAMINOOCTANE N-Boc-octane-1,8-diamine N1-Boc-octane-1,8-diamine TERT-BUTYL 8-AMINOOCTYLCARBAMATE 1,8-Diaminooctane, N1-BOC protected Octane-1,8-diamine, N-BOC protected tert-Butyl (8-aminooct-1-yl)carbamate N-t-Butyloxycarbonyl-1,8-diaminooctane Octane-1,8-diamine, N-BOC protected 95% 1,8-Diaminooctane, N1-BOC protected 95% N-tert-Butoxycarbonyl-1,8-octanediaMine Carbamic acid,N-(8-aminooctyl)-, 1,1-dimethylethyl ester tert-Butyl 8-aminooctylcarbamate
1,8-Diaminooctane N1-boc protected tert-Butyl (8-aminooct-1-yl)carbamate, 1,8-Diaminooctane, N-BOC protected | [Molecular Formula]
C13H28N2O2 | [MDL Number]
MFCD02094499 | [MOL File]
88829-82-7.mol | [Molecular Weight]
244.37 |
Hazard Information | Back Directory | [Description]
tert-butyl (8-aminooctyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs. tert-butyl (8-aminooctyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine. |
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