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18934-81-1

18934-81-1 Structure

18934-81-1 Structure
IdentificationBack Directory
[Name]

BOC-12-ADO-OH
[CAS]

18934-81-1
[Synonyms]

BOC-12-ADO-OH
BOC-NH-(CH2)11-COOH
BOC-12-AMINOLAURIC ACID
BOC-12-AMINODODECANOIC ACID
Boc-12-Ado-OH >=98.0% (TLC)
N-Boc-12-aminododecanoic acid
12-(BOC-AMINO)DODECANOIC ACID
T-BUTOXYCARBONYL-12-AMINOLAURIC ACID
T-BUTOXYCARBONYL-12-AMINODODECANOIC ACID
N-T-BUTYLOXYCARBONYL-12-AMINO-DODECANOIC ACID
N-tert-Butoxycarbonyl-12-aminododecanoic acid
N-TERT-BUTYLOXYCARBONYL-12-AMINO-DODECANOIC ACID
12-{[(tert-butoxy)carbonyl]amino}dodecanoic acid
12-[(2-methylpropan-2-yl)oxycarbonylamino]dodecanoic acid
Dodecanoic acid, 12-[[(1,1-dimethylethoxy)carbonyl]amino]-
[Molecular Formula]

C17H33NO4
[MDL Number]

MFCD00235887
[MOL File]

18934-81-1.mol
[Molecular Weight]

315.45
Chemical PropertiesBack Directory
[Melting point ]

83.5-84.5 °C
[Boiling point ]

454.5±18.0 °C(Predicted)
[density ]

0.997±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[form ]

powder
[pka]

4.78±0.10(Predicted)
[color ]

colorless to white
[BRN ]

1980302
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
[Uses]

Boc-12-Ado-OH can be used as a PROTAC linker in the synthesis of PROTACs. Boc-12-Ado-OH is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
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