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C70908

5-氯水杨酸

Name: 5-氯水杨酸
Brand: ALDRICH

98%

别名:

5-氯-2-羟基苯甲酸

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关于此项目

线性分子式:

ClC₆H₃(OH)CO₂H

化学文摘社编号:

321-14-2

分子量:

172.57

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24892929

EC Number:

206-283-9

Beilstein/REAXYS Number:

2046665

MDL number:

MFCD00002457

Assay:

98%

Form:

powder

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属性

Quality Level

100

assay

98%

form

powder

mp

171-172 °C (lit.)

SMILES string

OC(=O)c1cc(Cl)ccc1O

InChI

1S/C7H5ClO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)

InChI key

NKBASRXWGAGQDP-UHFFFAOYSA-N

Gene Information

human ... ALB(213)

说明

pictograms

GHS06

signalword

Danger

hcodes

H301

pcodes

P264 - P270 - P301 + P310 - P405 - P501

Hazard Classifications

Acute Tox. 3 Oral

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

历史批次信息供参考:

分析证书(COA)

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Comparative gastric ulcerogenic effects of meseclazone, 5-chlorosalicylic acid and other nonsteroidal anti-inflammatory drugs following acute and repeated oral administration to rats.

W Diamantis et al.

Toxicology and applied pharmacology, 52(3), 454-461 (1980-03-15)

Effect of biological confinement on the photophysics and dynamics of a proton-transfer phototautomer: an exploration of excitation and emission wavelength-dependent photophysics of the protein-bound drug.

Debarati Ray et al.

Physical chemistry chemical physics : PCCP, 14(35), 12182-12192 (2012-08-08)

The present work demonstrates the effect of biological confinement on the photophysics and dynamics of a bio-active drug molecule viz., 5-chlorosalicylic acid (5ClSA). 5ClSA is a potential candidate exhibiting Excited-State Intramolecular Proton Transfer (ESIPT) reaction and thereby generating the phototautomer

Microbial metabolism of chlorosalicylates: accelerated evolution by natural genetic exchange.

M A Rubio et al.

Archives of microbiology, 145(2), 116-122 (1986-07-01)

Methylsalicylate-grown cells of Pseudomonas sp. WR401 cometabolized 3-, 4- and 5-substituted halosalicylates to the corresponding halocatechols. Further degradation was unproductive due to the presence of high levels of catechol 2,3-dioxygenase. This strain acquired the ability to utilize 3-chlorobenzoate following acquisition

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全球贸易项目编号

货号	GTIN
C70908-100G	04061833511886