691445
4-Amino-3-chlorobenzoic acid
97%
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About This Item
Empirical Formula (Hill Notation):
C7H6ClNO2
CAS Number:
Molecular Weight:
171.58
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
219-630-4
MDL number:
InChI key
YIYBPEDZAUFQLO-UHFFFAOYSA-N
InChI
1S/C7H6ClNO2/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3H,9H2,(H,10,11)
SMILES string
Nc1ccc(cc1Cl)C(O)=O
assay
97%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
224-229 °C
application(s)
peptide synthesis
signalword
Warning
hcodes
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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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