55123-21-2 Usage
Description
(1R,5R,6R)-6-Methyl-2-methylene-6-(4-methyl-3-pentenyl)bicyclo[3.1.1]heptane is a complex bicyclic terpene compound derived from the isomerization of myrcene. It features a methyl and a methylene group within its structure, and is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Fragrance and Flavoring Industry:
(1R,5R,6R)-6-Methyl-2-methylene-6-(4-methyl-3-pentenyl)bicyclo[3.1.1]heptane is used as a fragrance or flavoring agent in the food and cosmetic industries. Its unique chemical structure contributes to its potential as a valuable ingredient in creating distinct scents and flavors.
Used in Organic Synthesis:
(1R,5R,6R)-6-Methyl-2-methylene-6-(4-methyl-3-pentenyl)bicyclo[3.1.1]heptane is used as a precursor in organic synthesis for the creation of more complex organic molecules. Its specific properties make it a promising candidate for developing new compounds with various applications.
Further research and analysis may be necessary to fully understand the potential uses and effects of this compound in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 55123-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,2 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55123-21:
(7*5)+(6*5)+(5*1)+(4*2)+(3*3)+(2*2)+(1*1)=92
92 % 10 = 2
So 55123-21-2 is a valid CAS Registry Number.
55123-21-2Relevant articles and documents
Synthesis of the racemate of (Z)-exo-alpha-bergamotenal, a pheromone component of the white-spotted spined bug, Eysarcoris parvus Uhler.
Alizadeh, Babak Heidary,Kuwahara, Shigefumi,Leal, Walter Soares,Men, Hong-Chao
, p. 1415 - 1418 (2007/10/03)
The racemate of (Z)-exo-alpha-bergamotenal, a sex pheromone component of the white-spotted spined bug, was synthesized from racemic exo-alpha-bergamotene by a five-step sequence involving regioselective epoxidation and (Z)-selective Wittig olefination reactions. The 1H- and 13C-NMR spectra of the synthetic sample were identical with those of the natural material.
SIMPLE SYNTHESIS OF (+)-β-TRANS-BERGAMOTENE
Corey, E. J.,Desai, Manoj C.
, p. 3535 - 3538 (2007/10/02)
(+)-β-trans-Bergamotene (4) has been synthesized in five steps from geranylacetone using intramolecular ketene-olefin cycloadditon as a key step.
Intramolecular Cycloadditions of Ketenes. 2. Synthesis of Crysanthenone, β-Pinene, β-cis-Bergamotene, and β-trans-Bergamotene
Kulkarni, Yashwant S.,Snider, Barry B.
, p. 2809 - 2810 (2007/10/02)
Vinylketenes prepared from geranoyl and farnesoyl chloride by treatment with triethylamine react to give bicycloheptanones which can be converted to β-pinene and the β-bergamotenes by Wolff-Kishner reduction.
