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Merck
모든 사진(1)

주요 문서

357782

Sigma-Aldrich

2,3,5-Trichlorobenzoic acid

97%

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About This Item

Linear Formula:
Cl3C6H2CO2H
CAS Number:
Molecular Weight:
225.46
Beilstein:
2097064
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
양식:
solid
분석:
97%

Quality Level

분석

97%

양식

solid

mp

166-167 °C (lit.)

작용기

carboxylic acid
chloro

SMILES string

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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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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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