Cas 155671-23-1,(S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one

155671-23-1

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Basic information

Product Name: (S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one
Synonyms: (S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one
CAS NO:155671-23-1
Molecular Formula:
Molecular Weight: 402.63
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: (S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one(155671-23-1)
EPA Substance Registry System: (S)-1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-3-((R)-toluene-4-sulfinyl)-propan-2-one(155671-23-1)

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: 155671-23-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155671-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,6,7 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155671-23:
(8*1)+(7*5)+(6*5)+(5*6)+(4*7)+(3*1)+(2*2)+(1*3)=141
141 % 10 = 1
So 155671-23-1 is a valid CAS Registry Number.

155671-23-1Upstream product

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155671-23-1Relevant academic research and scientific papers

Asymmetric synthesis monitored by chiral sulfoxides: Syn and anti functionalized 1,2-diols from α-hydroxy-esters

Solladie, Guy,Almario, Antonio

, p. 1937 - 1940 (2007/10/02)

The reduction of chiral b-keto-g-alkoxy-sulfoxides, readily made from chiral a-hydroxyesters, allowed the preparation of optically pure syn and anti functionalized 1,2-diols. The reduction is completely stereo controlled by the sulfoxide group.

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