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ChemicalBook--->CAS DataBase List--->111331-82-9

111331-82-9

111331-82-9 Structure

111331-82-9 Structure
IdentificationMore
[Name]

BOC-3-AMINOBENZOIC ACID
[CAS]

111331-82-9
[Synonyms]

3-(BOC-AMINO)BENZOIC ACID
3-(TERT-BUTYLOXYCARBONYLAMINO)-BENZOIC ACID
BOC-3-ABZ-OH
BOC-3-AMINOBENZOIC ACID
BOC-M-ABZ-OH
H-ALPHA-T-BUTOXYCARBONYL-3-AMINOBENZOIC ACID
N-ALPHA-T-BUTOXYCARBONYL-3-AMINOBENZOIC ACID
N-ALPHA-T-BUTOXYCARBONYL-M-AMINOBENZOIC ACID
3-(T-BUTYLOXYCARBONYLAMINO)-BENZOIC ACID
NALPHA-tert-Butoxycarbonyl-3-aminobenzoic acid
[Molecular Formula]

C12H15NO4
[MDL Number]

MFCD00235884
[Molecular Weight]

237.25
[MOL File]

111331-82-9.mol
Chemical PropertiesBack Directory
[Melting point ]

195 °C (dec.)
[Boiling point ]

339.8±25.0 °C(Predicted)
[density ]

1.242±0.06 g/cm3(Predicted)
[storage temp. ]

Store at 0-5°C
[pka]

4.15±0.10(Predicted)
[BRN ]

5813611
[CAS DataBase Reference]

111331-82-9(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29242990
Hazard InformationBack Directory
[Chemical Properties]

Brown powder
[Uses]

Boc-3-Abz-OH, is an intermediate in the synthesis of various pharmaceutical compounds, including inhibitors, and therapeutic agents. It can also be used in the preparation of conformationally-constrained cyclic peptides with biarylamine linkers.
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

111331-82-9(sigmaaldrich)
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