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Sigma-Aldrich

4-Amino-3-chlorobenzoic acid

97%

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About This Item

Empirical Formula (Hill Notation):
C7H6ClNO2
CAS Number:
2486-71-7
Molecular Weight:
171.58
EC Number:
219-630-4
MDL number:
MFCD00460423
UNSPSC Code:
12352106
eCl@ss:
32160406
PubChem Substance ID:
329761410

assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

224-229 °C

application(s)

peptide synthesis

SMILES string

Nc1ccc(cc1Cl)C(O)=O

InChI

1S/C7H6ClNO2/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3H,9H2,(H,10,11)

InChI key

YIYBPEDZAUFQLO-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Z W She et al.
Free radical biology & medicine, 22(6), 989-998 (1997-01-01)
This study was designed to develop traps for hypochlorous acid (HOCl) which could be used to detect HOCl in the microenvironment of activated neutrophils. Reagent HOCl was found to react with para-aminobenzoic acid (PABA) in aqueous solution to produce a
Tomasz Frączek et al.
Journal of enzyme inhibition and medicinal chemistry, 31(3), 481-489 (2015-05-06)
Azoles are a promising class of the new generation of HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). From thousands of reported compounds, many possess the same basic structure of an aryl substituted azole ring linked by a thioglycolamide chain with another

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