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Merck
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Key Documents

357782

Sigma-Aldrich

2,3,5-三氯苯甲酸

97%

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About This Item

線性公式:
Cl3C6H2CO2H
CAS號碼:
分子量::
225.46
Beilstein:
2097064
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

97%

形狀

solid

mp

166-167 °C (lit.)

官能基

carboxylic acid
chloro

SMILES 字串

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 密鑰

CGFDSIZRJWMQPP-UHFFFAOYSA-N

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象形圖

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訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Rearrangement of Halotropones. Chloride Exchange in Tribromotropolone.
Doering WE and Knox LH.
Journal of the American Chemical Society, 74(22), 5683-5687 (1952)
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)
Fatima El-Athman et al.
Environmental science and pollution research international, 26(31), 32636-32644 (2019-10-22)
Triiodinated benzoic acid derivatives are widely used as contrast media for medical examinations and are found at high concentrations in urban aquatic environments. During bank filtration, deiodination of iodinated contrast media has been observed under anoxic/anaerobic conditions. While several bacterial
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

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