71648-36-7 Usage
Explanation
1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl phenylacetate consists of 17 carbon atoms, 24 hydrogen atoms, and 2 oxygen atoms.
Explanation
The compound is typically a colorless to pale yellow liquid under normal conditions.
Explanation
Due to its hydrophobic nature, 1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl phenylacetate has limited solubility in water but dissolves well in organic solvents.
Explanation
1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl phenylacetate is commonly used in the production of pheromones and as a building block for the synthesis of related chemical compounds in the fragrance and flavor industry.
Explanation
The compound's complex structure includes a phenylacetate group attached to a cyclohexene ring, with a methyl and ethyl group attached to the cyclohexene.
Explanation
1-methyl-1-(4-methyl-3-cyclohexen-1-yl)ethyl phenylacetate is a member of the family of phenylacetates, which are known for their applications in the fragrance and flavor industry.
Explanation
The compound is also known as the Pheromone MCH (methylcyclohexene) analogue, which highlights its use in pheromone research and development.
Molecular weight
256.37 g/mol
Appearance
Colorless to pale yellow liquid
Solubility
Slightly soluble in water, soluble in organic solvents
Usage
Pheromone production, fragrance and flavor industry
Structure
Complex, consisting of a phenylacetate group, a cyclohexene ring, and methyl and ethyl groups
Family
Phenylacetates
Synonym
Pheromone MCH (methylcyclohexene) analogue
Check Digit Verification of cas no
The CAS Registry Mumber 71648-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,4 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71648-36:
(7*7)+(6*1)+(5*6)+(4*4)+(3*8)+(2*3)+(1*6)=137
137 % 10 = 7
So 71648-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O2/c1-14-9-11-16(12-10-14)18(2,3)20-17(19)13-15-7-5-4-6-8-15/h4-9,16H,10-13H2,1-3H3
71648-36-7Relevant academic research and scientific papers
NUCLEOPHILIC SUBSTITUTION OF ALKYL HALIDES BY ZINC SALTS-3 PREPARATION OF TERTARY ALKYL ESTERS AND ETHERS UNDER NON-SOLVOLYTIC CONDITIONS
Ravindranath, B.,Srinivas, P.
, p. 1623 - 1628 (2007/10/02)
Zinc salts of carboxylic acids, phenols and alcohols are found to react with tertiary alkyl halides in nonpolar solvents and in presence of a base yielding the corresponding esters and ethers in moderate to good yields.
