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ChemicalBook--->CAS DataBase List--->117445-22-4

117445-22-4

117445-22-4 Structure

117445-22-4 Structure
IdentificationMore
[Name]

Boc-3-Aminomethylbenzoic acid
[CAS]

117445-22-4
[Synonyms]

3-(BOC-AMINOMETHYL)BENZOIC ACID
3-(N-T-BUTYLOXYCARBONYLAMINOMETHYL)BENZOIC ACID
3-(TERT-BUTOXYCARBONYLAMINO-METHYL)-BENZOIC ACID
3-(TERT-BUTYLOXYCARBONYLAMINOMETHYL)-BENZOIC ACID
BOC-3-AMB-OH
BOC-3-AMINOMETHYLBENZOIC ACID
BOC-MAMB
BOC-MAMB-OH
RARECHEM EM WB 0054
3-(N-BOC-AMINOMETHYL)BENZOIC ACID
N-BOC-3-AMINOMETHYL-BENZOIC ACID
3-(t-Butyloxycarbonylaminomethyl)-benzoic acid
[EINECS(EC#)]

820-537-1
[Molecular Formula]

C13H17NO4
[MDL Number]

MFCD00273426
[Molecular Weight]

251.28
[MOL File]

117445-22-4.mol
Chemical PropertiesBack Directory
[Boiling point ]

434.6±38.0 °C(Predicted)
[density ]

1.178±0.06 g/cm3(Predicted)
[storage temp. ]

Store at 0°C
[form ]

Crystalline Powder or Flakes
[pka]

4.21±0.10(Predicted)
[color ]

White to off-white
[BRN ]

6957774
[CAS DataBase Reference]

117445-22-4(CAS DataBase Reference)
Safety DataBack Directory
[Safety Statements ]

24/25
[WGK Germany ]

3
[HazardClass ]

IRRITANT
[HS Code ]

29242990
Hazard InformationBack Directory
[Chemical Properties]

Off-white powder
[Uses]

3-(Boc-aminomethyl)benzoic Acid is used to synthesize aminodihydroquinazolines as inhibitors of BACE-1 (β-site APP cleaving enzyme). It is also used to prepare spiro[1H-indene-1,4''-piperidine] derivatives as potent and selective non-peptide human somatostatin receptor subtype 2 (sst2) agonists.
[reaction suitability]

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

117445-22-4(sigmaaldrich)
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