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Merck
CN

357782

Sigma-Aldrich

2,3,5-三氯苯甲酸

97%

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About This Item

线性分子式:
Cl3C6H2CO2H
CAS号:
分子量:
225.46
Beilstein:
2097064
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

mp

166-167 °C (lit.)

SMILES字符串

OC(=O)c1cc(Cl)cc(Cl)c1Cl

InChI

1S/C7H3Cl3O2/c8-3-1-4(7(11)12)6(10)5(9)2-3/h1-2H,(H,11,12)

InChI key

CGFDSIZRJWMQPP-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Effects of temperature on biological degradation of phenols, benzoates and phthalates under methanogenic conditions.
Leven L and Schnurer A.
International Biodeterioration & Biodegradation, 55(2), 153-160 (2005)
Rearrangement of Halotropones. Chloride Exchange in Tribromotropolone.
Doering WE and Knox LH.
Journal of the American Chemical Society, 74(22), 5683-5687 (1952)
Meng Qi et al.
Analytical and bioanalytical chemistry, 412(25), 6995-7006 (2020-08-02)
Dicamba herbicide is increasingly used in the world, in particular' with the widespread cultivation of genetically modified dicamba-resistant crops. However, the drift problem in the field has caused phytotoxicity against naive, sensitive crops, raising legal concerns. Thus, it is particularly
Prakash Karegoudar et al.
European journal of medicinal chemistry, 43(4), 808-815 (2007-09-07)
The reaction of 2,3,5-trichlorobenzoic acid hydrazide with carbon disulfide and potassium hydroxide followed by treatment with hydrazine hydrate afforded 3-(2,3,5-trichlorophenyl)-4-amino-1,2,4-triazole-5-thione (6). Alternatively, this triazole was also synthesized by fusing 2,3,5-trichlorobenzoic acid with thiocarbohydrazide. Condensation of (6) with various aromatic carboxylic
Emeline L Maillet et al.
Journal of medicinal chemistry, 52(21), 6931-6935 (2009-10-13)
We show that phenoxyauxin herbicides and lipid-lowering fibrates inhibit human but not rodent T1R3. T1R3 as a coreceptor in taste cells responds to sweet compounds and amino acids; in endocrine cells of gut and pancreas T1R3 contributes to glucose sensing.

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