Cas 472-76-4,3-Buten-1-ol, 4-(2,2-dimethyl-6-methylenecyclohexyl)-

472-76-4

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Basic information

Product Name: 3-Buten-1-ol, 4-(2,2-dimethyl-6-methylenecyclohexyl)-
Synonyms:
CAS NO:472-76-4
Molecular Formula: C13H22O
Molecular Weight: 194.317
EINECS: N/A
Product Categories: N/A
Mol File: 472-76-4.mol

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: 3-Buten-1-ol, 4-(2,2-dimethyl-6-methylenecyclohexyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Buten-1-ol, 4-(2,2-dimethyl-6-methylenecyclohexyl)-(472-76-4)
EPA Substance Registry System: 3-Buten-1-ol, 4-(2,2-dimethyl-6-methylenecyclohexyl)-(472-76-4)

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: 472-76-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 472-76-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 472-76:
(5*4)+(4*7)+(3*2)+(2*7)+(1*6)=74
74 % 10 = 4
So 472-76-4 is a valid CAS Registry Number.

472-76-4Upstream product

472-76-4Downstream Products

79-76-5 γ-ionone

472-76-4Relevant academic research and scientific papers

Synthesis and olfactory evaluation of the enantiomerically enriched forms of 7,11-epoxymegastigma-5(6)-en-9-one and 7,11-epoxymegastigma-5(6)-en-9-ols isomers, identified in Passiflora edulis

Brenna, Elisabetta,Fuganti, Claudio,Serra, Stefano

, p. 1699 - 1704 (2005)

A study on the synthesis of the isomers of the natural C-13 norterpenoids derivatives 7,11-epoxymegastigma-5(6)-en-9-one and 7,11-epoxymegastigma-5(6)-en- 9-ols is reported. The latter compounds were prepared from readily available racemic α-ionone and then resolved by mean of lipase-mediated acetylation. The obtained enantiomerically forms were evaluated for their odour properties.

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