Identification | Back Directory | [Name]
1-BOC-1,10-DIAMINODECANE | [CAS]
216961-61-4 | [Synonyms]
Boc-DADec 1-BOC-1,10-DIAMINODECANE N-Boc-decane-1,10-diamine 1-Boc-decane-1,10-diamine TERT-BUTYL 10-AMINODECYLCARBAMATE 1,10-DIAMINODECANE, N1-BOC PROTECTED Decane-1,10-diamine, N-BOC protected Decane-1,10-diamine,N-BOCprotected97% N-t-Butyloxycarbonyl-1,10-diaminodecane Decane-1,10-diamine, N-BOC protected 97% 1,10-Diaminodecane, N1-BOC protected 97% (13-amino-2-methyltridecan-2-yl)carbamic acid Carbamic acid,N-(10-aminodecyl)-, 1,1-dimethylethyl ester tert-Butyl (10-aminodec-1-yl)carbamate, 1,10-Diaminodecane, N-BOC protected | [Molecular Formula]
C15H32N2O2 | [MDL Number]
MFCD02094501 | [MOL File]
216961-61-4.mol | [Molecular Weight]
272.43 |
Chemical Properties | Back Directory | [Boiling point ]
380.4±15.0 °C(Predicted) | [density ]
0.932±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
12.94±0.46(Predicted) |
Hazard Information | Back Directory | [Description]
tert-Butyl (10-aminodecyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. tert-Butyl (10-aminodecyl)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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Rhawn Reagent
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