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625-01-4

625-01-4

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625-01-4 Usage

Chemical Properties

Colorless, oily liquid; pungent odor.Fumes in moist air. Decomposed by water. Attacks lead and tin but copper only mildly; iron and steel not affected. Soluble in chloroform and ether; insoluble in water.

Uses

Organic synthesis, military poison.

Hazard

Strong irritant to eyes and skin, evolves phosgene when heated.

Check Digit Verification of cas no

The CAS Registry Mumber 625-01-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 625-01:
(5*6)+(4*2)+(3*5)+(2*0)+(1*1)=54
54 % 10 = 4
So 625-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C2H5ClO3S/c1-2-6-7(3,4)5/h2H2,1H3

625-01-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorosulfonyloxyethane

1.2 Other means of identification

Product number -
Other names ethyl sulfurochloridate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:625-01-4 SDS

625-01-4Relevant articles and documents

Buncel,Millington

, p. 556,562 (1965)

Synthesis, characterization and in vitro anti-tumor activities of matrine derivatives

Wang, Lisheng,You, Yejun,Wang, Songqing,Liu, Xu,Liu, Buming,Wang, Jinni,Lin, Xiao,Chen, Mingsheng,Liang, Gang,Yang, Hua

supporting information; experimental part, p. 4100 - 4102 (2012/07/14)

Nineteen previously unreported matrine derivatives were synthesized and characterized using elemental analysis, infrared spectroscopy, proton nuclear magnetic resonance spectroscopy, and mass spectrometry. Target compounds 6a-6l and 7a-7c showed stronger inhibitory activities than matrine in the in vitro antitumor tests and inhibited the growth of the Hep7402, B16-F10, A549, and TW03 cell lines. In addition, compound 6i exhibited a potent antitumor activity similar to that of colchicine.

On the esters of thiosulfurous acid.

ZINNER,KOELLING

, p. 284 - 291 (2007/10/05)

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