136808-51-0 Usage
General Description
1-Propanol, 2-chloro-3-(phenylthio)-, acetate is a chemical compound with the molecular formula C10H11ClO2S. It is an ester formed from 1-propanol and 2-chloro-3-(phenylthio)acetic acid. 1-Propanol, 2-chloro-3-(phenylthio)-, acetate is used as an intermediate in organic synthesis and is commonly used for laboratory research purposes. It is a colorless liquid with a strong, pungent odor and is considered to be moderately toxic if ingested, inhaled, or absorbed through the skin. 1-Propanol, 2-chloro-3-(phenylthio)-, acetate should be handled with care and used in a well-ventilated area to avoid any potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 136808-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136808-51:
(8*1)+(7*3)+(6*6)+(5*8)+(4*0)+(3*8)+(2*5)+(1*1)=140
140 % 10 = 0
So 136808-51-0 is a valid CAS Registry Number.
136808-51-0Relevant academic research and scientific papers
Palladium- and light-enhanced ring-opening of oxiranes by copper chloride
Muzart, Jacques,Riahi, Abdelkhalek
, p. 323 - 336 (2007/10/02)
The yields of chlorohydrins formed by cleavage of epoxides by CuCl2 is increased in the presence of small amounts of PdCl2(MeCN)2.The conversion drops dramatically on carrying out the reaction in the dark.The regiochemistry of the ring-opening is sensitive to the nature of the substituents.
FUNCTIONALLY SUBSITUTED SULFUR-CONTAINING COMPOUNDS. 9. REASTIONS OF 2-OXIRANES WITH ACETIC ANHYDRIDE AND ACETYL CHLORIDE
Kalugin, V. E.,Litvinov, V. P.
, p. 1391 - 1394 (2007/10/02)
Reaction of 2-oxiranes with acetic anhydride gives a mixture of 3-(organylthio)-1,2-diacetoxypropane and 2-(organylthio)-1,3-diacetoxypropane, and with acetyl chloride a mixture of 2-chloro-3-(organylthio)-1-acetoxypropane and 3-chloro-2-(organylthio)-1-acetoxypropane.In both cases, the ratio of the isomers depends on the nature of the organylthio group and on the nature of the electrophile.
