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216961-61-4

216961-61-4 Structure

216961-61-4 Structure
IdentificationBack 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 PropertiesBack 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
[form ]

solid
[pka]

12.94±0.46(Predicted)
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335
[Precautionary statements ]

P261-P271-P280
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2924190090
Hazard InformationBack 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.
[Uses]

tert-Butyl (10-aminodecyl)carbamate (1-Boc-1,10-diaminodecane) 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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