Cas 161265-08-3,tert-Butyl-((1R,2S)-2-ethylsulfanyl-1-phenyl-2-p-tolylsulfanyl-ethoxy)-dimethyl-silane

161265-08-3

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Basic information

Product Name: tert-Butyl-((1R,2S)-2-ethylsulfanyl-1-phenyl-2-p-tolylsulfanyl-ethoxy)-dimethyl-silane
Synonyms:
CAS NO:161265-08-3
Molecular Formula:
Molecular Weight: 418.74
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: tert-Butyl-((1R,2S)-2-ethylsulfanyl-1-phenyl-2-p-tolylsulfanyl-ethoxy)-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-Butyl-((1R,2S)-2-ethylsulfanyl-1-phenyl-2-p-tolylsulfanyl-ethoxy)-dimethyl-silane(161265-08-3)
EPA Substance Registry System: tert-Butyl-((1R,2S)-2-ethylsulfanyl-1-phenyl-2-p-tolylsulfanyl-ethoxy)-dimethyl-silane(161265-08-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 161265-08-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161265-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,6 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 161265-08:
(8*1)+(7*6)+(6*1)+(5*2)+(4*6)+(3*5)+(2*0)+(1*8)=113
113 % 10 = 3
So 161265-08-3 is a valid CAS Registry Number.

161265-08-3Upstream product

75-08-1 ethanethiol

161265-08-3Downstream Products

161265-08-3Relevant academic research and scientific papers

A NOVEL DIASTEREOSELECTIVE SYNTHESIS OF CHIRAL, NON-RACEMIC UNSYMMETRICAL THIOACETALS USING SILICON-INDUCED PUMMERER-TYPE REACTION

Shibata, Norio,Fujita, Shigekazu,Gyoten, Michiyo,Matsumoto, Keita,Kita, Yasuyuki

, p. 109 - 112 (1995)

Chiral, non-racemic sulfoxides were reacted with thiols and BSA in the presence of a catalytic amount of TMSOTf in MeCN at rt overnight to give the corresponding chiral, non-racemic anti-thioacetals with high diastereoselectivity.

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