Cat. No JK346832_100_G
J&K Chemical

Product Information

Product Name
2-Amino-4-chlorobenzoic acid, 98%
Brand Name
J&K
Product Number
346832
CAS
89-77-0
Molecular Formula
C7H6ClNO2
Molecular Weight
171.58
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
4-Chloroanthranilic acid
PubChem CID
66646
IUPAC Name
2-amino-4-chlorobenzoic acid
InChI Key
JYYLQSCZISREGY-UHFFFAOYSA-N
SMILES
C1=CC(=C(C=C1Cl)N)C(=O)O

Properties

Melting Point
231-233

Safety Information

Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

Synthesis of Phthaladyn-29 and Naphthalimide-10, GTP Site Directed Dynamin GTPase Inhibitors

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2022
DOI: 10.1007/978-1-0716-1916-2_18

Synthesis from Ethyl 2-(4-Oxo-4H-benzo[d][1,3]oxazin-2-yl)acetate

Publication Name: Science of Synthesis
Publication Date: 2022

Selenium-catalyzed intramolecular atom- and redox-economical transformation ofo-nitrotoluenes into anthranilic acids

Publication Name: Green Chemistry
Publication Date: 2021
DOI: 10.1039/d0gc04407e

Synthesis, In Vitro Antiproliferative Activity, and In Silico Studies of New Anilinoquinazoline Derivatives as Potential AntitumorAgents

Publication Name: Russian Journal of General Chemistry
Publication Date: 2020-12
DOI: 10.1134/s1070363220120294

Kumada Cross Coupling Reaction for the Synthesis of Quinazoline Derivatives, Evaluation of Their Antibacterial Activity and Docking Studies

Publication Name: Russian Journal of General Chemistry
Publication Date: 2019-12
DOI: 10.1134/s107036321912034x

2-Amino-4-chlorobenzoic acid, 98%

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