146110
3,5-二氯-2-羟基苯磺酰氯
99%
别名:
2,4-二氯苯酚-6-磺酰氯
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关于此项目
线性分子式:
Cl2C6H2(OH)SO2Cl
化学文摘社编号:
分子量:
261.51
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
245-619-9
Beilstein/REAXYS Number:
2940993
MDL number:
产品名称
3,5-二氯-2-羟基苯磺酰氯, 99%
InChI
1S/C6H3Cl3O3S/c7-3-1-4(8)6(10)5(2-3)13(9,11)12/h1-2,10H
InChI key
KXFQRJNVGBIDHA-UHFFFAOYSA-N
SMILES string
Oc1c(Cl)cc(Cl)cc1S(Cl)(=O)=O
assay
99%
mp
80-83 °C (lit.)
functional group
chloro
Quality Level
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Application
3,5-Dichloro-2-hydroxybenzenesulfonyl chloride was used in the synthesis of (1R,2R)-(+)-1,2-(3,3′,5,5′-tetrachloro-2,2′-dihydroxydibenzenesulfonamido)-1,2-diphenylethane and (1R,2R)-(+)- 1,2-(3,3′,5,5′-tetrachloro-2,2′-dihydroxydibenzenesulfonamido)cyclohexane. It was used as chromogenic system in one-step kinetic method for the determination of 5′-nucleotidase.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
A Bertrand et al.
Clinica chimica acta; international journal of clinical chemistry, 119(3), 275-284 (1982-03-12)
We describe a one-step kinetic method for the determination of 5'-nucleotidase (EC 3.1.3.5). Inosine is formed by the hydrolysis of inosine 5'-monophosphate which is catalyzed by seric 5'-nucleotidase, and then is converted to hypoxanthine by nucleoside phosphorylase. Two moles of
Enantioselective addition of diethylzinc to benzaldehyde catalyzed by chiral titanate complexes with helical ligands.
Guo C, et al.
Tetrahedron, 53(12), 4145-4158 (1997)
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