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Merck
CN

15299

Boc-4-Abz-OH

≥98.0% (T)

Synonym(s):

4-(Boc-amino)benzoic acid

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About This Item

Linear Formula:
(CH3)3CO2CNHC6H4CO2H
CAS Number:
Molecular Weight:
237.25
PubChem Substance ID:
UNSPSC Code:
12352209
Beilstein/REAXYS Number:
2115614
MDL number:
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Product Name

Boc-4-Abz-OH, ≥98.0% (T)

SMILES string

CC(C)(C)OC(=O)Nc1ccc(cc1)C(O)=O

InChI

1S/C12H15NO4/c1-12(2,3)17-11(16)13-9-6-4-8(5-7-9)10(14)15/h4-7H,1-3H3,(H,13,16)(H,14,15)

InChI key

ZJDBQMWMDZEONW-UHFFFAOYSA-N

assay

≥98.0% (T)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

~200 °C (dec.)

application(s)

peptide synthesis

Other Notes

BOC-protected derivative of PABA.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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M H Norman et al.
Journal of medicinal chemistry, 39(5), 1172-1188 (1996-03-01)
A series of substituted (4-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)butyl)benzamide derivatives was prepared and evaluated as potential atypical antipsychotic agents. The target compounds were readily prepared from their benzoyl chloride, benzoic acid, or isatoic anhydride precursors, and they were evaluated in vitro for their ability

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