| Identification | Back 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 Properties | Back 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) | [BRN ]
1980302 |
| Hazard Information | Back 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. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
|
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Sigma-Aldrich
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Shanghai GL Peptide Ltd.
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