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Merck

252700

Sigma-Aldrich

4-(氯磺酰基)苯甲酸

96%

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1 G
$55.40
5 G
$74.40
25 G
$220.00

About This Item

线性分子式:
ClSO2C6H4CO2H
CAS号:
分子量:
220.63
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

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方案

96%

表单

solid

mp

233-235 °C (lit.)

官能团

carboxylic acid

SMILES字符串

OC(=O)c1ccc(cc1)S(Cl)(=O)=O

InChI

1S/C7H5ClO4S/c8-13(11,12)6-3-1-5(2-4-6)7(9)10/h1-4H,(H,9,10)

InChI key

PTCSSXYPZOFISK-UHFFFAOYSA-N

应用

4-(Chlorosulfonyl)benzoic acid was used in the preparation of polymer bound transfer hydrogenation catalyst[1] and 4-(carboxymethyl-sulfamoyl)-benzoyladenosine[2]. It was also used as a reagent in the sulfonation of γ-cyclodextrin[3].

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Synthesis and evaluation of a chiral heterogeneous transfer hydrogenation catalyst.
Bayston DJ, et al.
Tetrahedron Asymmetry, 9(12), 2015-2018 (1998)
Mono-6-(O-2, 4, 6-triisopropylbenzenesulfonyl)-?-cyclodextrin, a novel intermediate for the synthesis of mono-functionalised ?-cyclodextrins.
Palin R, et al.
Tetrahedron Letters, 42(50), 8897-8899 (2001)
Nguyen-Hai Nam et al.
Bioorganic & medicinal chemistry, 12(22), 5753-5766 (2004-10-23)
A number of Src SH2 domain inhibitors enhance the kinase catalytic activity by switching the closed inactive to the open active conformation. ATP-phosphopeptide conjugates were designed and synthesized as Src tyrosine kinase inhibitors based on a tetrapeptide sequence pTyr-Glu-Glu-Ile (pYEEI)

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