Cas 117180-83-3,(2R*,4S*,5R*)-(+/-)-5-Ethyl-2-methyl-2-<2-(phenylsulfonyl)ethyl>-4-(tosyloxymethyl)-1,3-dioxolan

117180-83-3

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Basic information

Product Name: (2R*,4S*,5R*)-(+/-)-5-Ethyl-2-methyl-2-<2-(phenylsulfonyl)ethyl>-4-(tosyloxymethyl)-1,3-dioxolan
Synonyms:
CAS NO:117180-83-3
Molecular Formula:
Molecular Weight: 468.592
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: (2R*,4S*,5R*)-(+/-)-5-Ethyl-2-methyl-2-<2-(phenylsulfonyl)ethyl>-4-(tosyloxymethyl)-1,3-dioxolan(CAS DataBase Reference)
NIST Chemistry Reference: (2R*,4S*,5R*)-(+/-)-5-Ethyl-2-methyl-2-<2-(phenylsulfonyl)ethyl>-4-(tosyloxymethyl)-1,3-dioxolan(117180-83-3)
EPA Substance Registry System: (2R*,4S*,5R*)-(+/-)-5-Ethyl-2-methyl-2-<2-(phenylsulfonyl)ethyl>-4-(tosyloxymethyl)-1,3-dioxolan(117180-83-3)

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: 117180-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 117180-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,1,8 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 117180-83:
(8*1)+(7*1)+(6*7)+(5*1)+(4*8)+(3*0)+(2*8)+(1*3)=113
113 % 10 = 3
So 117180-83-3 is a valid CAS Registry Number.

117180-83-3Upstream product

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117180-83-3Relevant academic research and scientific papers

Stereoselective Acetalization of 1,1- and 1,2-Disubstituted Diols as Common Principle in the Synthesis of the Enantiomers of the Bicyclic Acetal Pheromones endo- and exo-Brevicomin and Frontalin

Wershofen, Stefan,Classen, Arnold,Scharf, Hans-Dieter

, p. 9 - 18 (2007/10/02)

The acetalization of the 1,1- and 1,2-disubstituted diols 14-19 with the keto compounds 20 and 21 has been investigated.The substitution pattern of the used diols shows great influence on the stereochemistry of the obtained dioxolanes 22-27 (mixtures of d

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