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ChemicalBook--->CAS DataBase List--->60142-89-4

60142-89-4

60142-89-4 Structure

60142-89-4 Structure
IdentificationMore
[Name]

BOC-7-AMINO-HEPTANOIC ACID
[CAS]

60142-89-4
[Synonyms]

7-(BOC-AMINO)ENANTHIC ACID
7-(BOC-AMINO)HEPTANOIC ACID
BOC-7-AHP-OH
BOC-7-AMINO-HEPTANOIC ACID
BOC-AHEPT-OH
BOC-NH-(CH2)6-COOH
N-BOC-7-AMINOHEPTANOIC ACID
N-T-BUTOXYCARBONYL-7-AMINOENANTHIC ACID
N-T-BUTOXYCARBONYL-7-AMINOHEPTANOIC ACID
N-TERT-BUTYLOXYCARBONYL-7-AMINOHEPTANOIC ACID
7-Aminoheptanoic acid, N-BOC protected
N-tert-Butoxycarbonyl-7-aminoheptanoic acid
7-(Boc-amino)enanthic acid, 7-(Boc-amino)heptanoic acid, Boc-7-aminoheptanoic acid
[Molecular Formula]

C12H23NO4
[MDL Number]

MFCD00063356
[Molecular Weight]

245.32
[MOL File]

60142-89-4.mol
Chemical PropertiesBack Directory
[Melting point ]

56-60 °C
[Boiling point ]

393.1±25.0 °C(Predicted)
[density ]

1.050±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

soluble in Methanol
[form ]

powder to crystaline
[pka]

4.77±0.10(Predicted)
[color ]

White to Almost white
[BRN ]

2050867
[CAS DataBase Reference]

60142-89-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

3
[F ]

9-21
[HS Code ]

2922.50.5000
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Description]

Boc-7-Aminoheptanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Boc-7-Aminoheptanoic acid 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
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

60142-89-4(sigmaaldrich)
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