625-01-4 Usage
Description
ETHYL CHLOROSULFONATE is a colorless, oily liquid with a pungent odor. It fumes in moist air and is decomposed by water. It attacks lead and tin but has a mild effect on copper; iron and steel are not affected by it. ETHYL CHLOROSULFONATE is soluble in chloroform and ether but insoluble in water. It is primarily used in organic synthesis and has applications in the military as a poison.
Uses
Used in Organic Synthesis:
ETHYL CHLOROSULFONATE is used as a reagent in the field of organic synthesis for its ability to facilitate various chemical reactions and produce desired products.
Used in Military Applications:
ETHYL CHLOROSULFONATE is used as a chemical warfare agent in the military due to its toxic properties. Its use in this context is highly regulated and subject to international agreements and restrictions.
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
625-01-4Relevant 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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