推荐产品
化驗
99%
mp
80-83 °C (lit.)
SMILES 字串
Oc1c(Cl)cc(Cl)cc1S(Cl)(=O)=O
InChI
1S/C6H3Cl3O3S/c7-3-1-4(8)6(10)5(2-3)13(9,11)12/h1-2,10H
InChI 密鑰
KXFQRJNVGBIDHA-UHFFFAOYSA-N
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應用
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.
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
儲存類別代碼
8A - Combustible corrosive hazardous materials
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
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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.
Tetrahedron, 53(12), 4145-4158 (1997)
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