Cas 308122-93-2,(1S,2S,4R)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol

308122-93-2

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Basic information

Product Name: (1S,2S,4R)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol
Synonyms: (1S,2S,4R)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol
CAS NO:308122-93-2
Molecular Formula:
Molecular Weight: 314.492
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)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,4R)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol(308122-93-2)
EPA Substance Registry System: (1S,2S,4R)-7,7-dimethyl-1-[(Z)-2-(phenylthio)vinyl]-2-[(Z)-1-propenyl]bicyclo[2.2.1]heptan-2-ol(308122-93-2)

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: 308122-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 308122-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,1,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 308122-93:
(8*3)+(7*0)+(6*8)+(5*1)+(4*2)+(3*2)+(2*9)+(1*3)=112
112 % 10 = 2
So 308122-93-2 is a valid CAS Registry Number.

308122-93-2Upstream product

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308122-93-2Relevant academic research and scientific papers

High-rate accelerations in oxy-Cope rearrangements induced by sulfur substitution: Kinetic study involving electronically and geometrically differentiated 1-alkenyl-2-(Z-1-propenyl)-7,7-dimethyl-exo-norbornan-2-ols

Paquette,Reddy,Vayner,Houk

, p. 10788 - 10794 (2007/10/03)

The rates of anionically promoted oxy-Cope rearrangement of five structurally related exonorbornanols have been determined. A critical difference in the substitution pattern of these substrates is the presence or absence of oxygen or sulfur functionality

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