ChemicalBook--->CAS DataBase List--->173435-78-4

173435-78-4

173435-78-4 Structure

173435-78-4 Structure
IdentificationBack Directory
[Name]

BOC-9-AMINONONANOIC ACID
[CAS]

173435-78-4
[Synonyms]

BOC-9-ANC-OH
Boc-9-aminononane acid
BOC-9-AMINONONANOIC ACID
9-(Boc-amino)-nonanoic acid
Boc-9-aminononanoic acid≥ 98% (HPLC)
N-T-BUTYLOXYCARBONYL-9-AMINO-NONANOIC ACID
9-((tert-Butoxycarbonyl)aMino)nonanoic acid
N-TERT-BUTYLOXYCARBONYL-9-AMINO-NONANOIC ACID
Nonanoic acid, 9-[[(1,1-dimethylethoxy)carbonyl]amino]-
[Molecular Formula]

C14H27NO4
[MDL Number]

MFCD02092968
[MOL File]

173435-78-4.mol
[Molecular Weight]

273.37
Chemical PropertiesBack Directory
[Boiling point ]

418.8±28.0 °C(Predicted)
[density ]

1.025±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

4.78±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard InformationBack Directory
[Description]

9-(Boc-amino)nonanoic Acid is an alkane chain with terminal carboxlic acid and Boc-protected amino groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. 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.
[Chemical Properties]

White solid
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