Cas 131934-40-2,(1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol

131934-40-2

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Basic information

Product Name: (1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol
Synonyms: (1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol
CAS NO:131934-40-2
Molecular Formula:
Molecular Weight: 306.445
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: (1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol(131934-40-2)
EPA Substance Registry System: (1S,2S,4R)-2-((S)-3-Methoxymethoxy-cyclohex-1-enyl)-7,7-dimethyl-1-vinyl-bicyclo[2.2.1]heptan-2-ol(131934-40-2)

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: 131934-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131934-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,3 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131934-40:
(8*1)+(7*3)+(6*1)+(5*9)+(4*3)+(3*4)+(2*4)+(1*0)=112
112 % 10 = 2
So 131934-40-2 is a valid CAS Registry Number.

131934-40-2Upstream product

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131934-40-2Relevant academic research and scientific papers

Impact of substituent modifications on the atropselectivity characteristics of an anionic oxy-Cope ring expansion

Raquette, Leo A.,Combrink, Keith D.,Elmore, Steven W.,Rogers, Robin D.

, p. 1335 - 1344 (2007/10/02)

The phenomenon of atropisomerism is critically examined in the tricyclic E,syn,up enolates derived from anionic oxy-Cope rearrangement of 1-vinyl-2-cyclohexenyl-7,7-dimethyl-exo-norbornan-2-ols, as well as the ketones derived from their protonation and me

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