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145793

Sigma-Aldrich

4-Chloro-2-methoxybenzoic acid

99%

Synonym(s):

4-Chloro-o-anisic acid

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About This Item

Linear Formula:
ClC6H3(OCH3)CO2H
CAS Number:
Molecular Weight:
186.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

99%

form

powder

mp

146-148 °C (lit.)

functional group

carboxylic acid
chloro

SMILES string

COc1cc(Cl)ccc1C(O)=O

InChI

1S/C8H7ClO3/c1-12-7-4-5(9)2-3-6(7)8(10)11/h2-4H,1H3,(H,10,11)

InChI key

UFEYMXHWIHFRBX-UHFFFAOYSA-N

General description

4-Chloro-2-methoxybenzoic acid anion forms complexes with Mn2+, Co2+, Ni2+, Cu2+ and Zn2+[1].

Application

4-Chloro-2-methoxybenzoic acid was used in the synthesis of (2-(4-chloro-2-methoxybenzoyl)-1′H-1,3′-bipyrrol-2′-yl)(2-methoxyphenyl)methanone[2].

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Yan Liu et al.
Marine drugs, 10(4), 953-962 (2012-06-13)
Infections caused by drug-resistant pathogens are on the rise. The ongoing spread of methicillin-resistant Staphylococcus aureus (MRSA) strains exemplifies the urgent need for new antibiotics. The marine natural product, marinopyrrole A, was previously shown to have potent antibiotic activity against
Complexes of Mn (II), Co (II), Ni (II), Cu (II) and Zn (II) with 4-chloro-2-methoxybenzoic acid anion.
Ferenc, et al.
Journal of Thermal Analysis and Calorimetry, 86(3), 783-789 (2006)

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