Cas 71539-59-8,[5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one

71539-59-8

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Product Name: [5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one
Synonyms: (+)-Bis-trans-ocimenone;(5E)-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexen-1α-yl]-2,5-heptadien-4-one;[5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexen-1α-yl]-2,5-heptadien-4-one;[5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one;Bis-trans-Ocimenone
CAS NO:71539-59-8
Molecular Formula: C₂₀H₂₈O₂
Molecular Weight: 300.43512
EINECS: N/A
Product Categories: N/A
Mol File: 71539-59-8.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: [5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one(CAS DataBase Reference)
NIST Chemistry Reference: [5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one(71539-59-8)
EPA Substance Registry System: [5E,(+)]-2-Methyl-6-[(1S)-3-methyl-2α-(3-methyl-1-oxo-2-butenyl)-3-cyclohexene-1α-yl]-2,5-heptadiene-4-one(71539-59-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 71539-59-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 71539-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,3 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 71539-59:
(7*7)+(6*1)+(5*5)+(4*3)+(3*9)+(2*5)+(1*9)=138
138 % 10 = 8
So 71539-59-8 is a valid CAS Registry Number.

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71539-59-8Relevant academic research and scientific papers

Terpenes and Terpene Derivatives, XVII. - Thermal and AlCl3-Catalyzed Reaction of Ocimenone

Weyerstahl, Peter,Zombik, Winfried,Gansau, Christian

, p. 422 - 427 (2007/10/02)

Bis(trans-ocimenone) (5),reported to be a naturally occuring compound, is formed by thermal dimerization of (E)-ocimenone (E-4). - Treatment of 4 with AlCl3 leads, in addition to unchanged 4, to a mixture of the rearranged products filifolone (6) and rac-

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