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线性分子式:
ClC6H3(OCH3)CO2H
化学文摘社编号:
分子量:
186.59
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
260-761-1
MDL number:
Assay:
99%
Form:
powder
产品名称
4-氯-2-甲氧基苯甲酸, 99%
InChI key
UFEYMXHWIHFRBX-UHFFFAOYSA-N
InChI
1S/C8H7ClO3/c1-12-7-4-5(9)2-3-6(7)8(10)11/h2-4H,1H3,(H,10,11)
SMILES string
COc1cc(Cl)ccc1C(O)=O
assay
99%
form
powder
mp
146-148 °C (lit.)
functional group
carboxylic acid
chloro
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.
General description
4-Chloro-2-methoxybenzoic acid anion forms complexes with Mn2+, Co2+, Ni2+, Cu2+ and Zn2+.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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