Cas 1025022-71-2,Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester

1025022-71-2

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Basic information

Product Name: Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester
Synonyms: Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester
CAS NO:1025022-71-2
Molecular Formula:
Molecular Weight: 384.54
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: Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester(1025022-71-2)
EPA Substance Registry System: Z-(RS,2S)-2,4-dimethyl-3-(p-tolylsulfinylmethylene)-pentanoic acid 2,6-dimethylphenyl ester(1025022-71-2)

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: 1025022-71-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1025022-71-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,0,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1025022-71:
(9*1)+(8*0)+(7*2)+(6*5)+(5*0)+(4*2)+(3*2)+(2*7)+(1*1)=82
82 % 10 = 2
So 1025022-71-2 is a valid CAS Registry Number.

1025022-71-2Upstream product

888734-77-8 (SS,SS,2S,3R)-3-[bis-(p-tolylsulfinyl)-methyl]-2,4-dimethylpentanoic acid 2,6-dimethylphenyl ester

1025022-71-2Downstream Products

1025022-71-2Relevant academic research and scientific papers

Diastereoselective synthesis of enantiopure acyclic ss,ss -disubstituted vinylsulfoxides

Brebion, Franck,Goddard, Jean-Philippe,Fensterbank, Louis,Malacria, Max

supporting information; experimental part, p. 1917 - 1920 (2009/04/18)

Thermal elimination of sulfenic acid from enantiopure ss,ss -disubstituted bis-sulfoxides allows the stereoselective synthesis of enantiopure acyclic ss,ss -disubstituted vinylsulfoxides. This mild and stereospecific synthesis provides either (E) or (Z) v

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