81968-65-2 Usage
Description
[2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate is a complex organic compound characterized by a cyclopropyl ring, a methyl acetate group, and a 2-methylpropenyl group. Its unique structure, which includes a cyclopropyl ring and a 2-methylpropenyl group, suggests potential applications in various fields, including synthetic organic chemistry, pharmaceuticals, and agrochemicals. [2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate's distinctive architecture may also render it a valuable building block for the synthesis of more intricate molecules.
Uses
Used in Synthetic Organic Chemistry:
[2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate is used as a synthetic intermediate for the creation of more complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a promising candidate for the development of novel compounds with specific properties and applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, [2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate is used as a key component in the synthesis of new drugs. Its structural features may contribute to the development of innovative therapeutic agents with improved efficacy and selectivity.
Used in Agrochemicals:
[2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate is used as a building block in the design and synthesis of new agrochemicals, such as pesticides and herbicides. Its unique structural elements could potentially enhance the effectiveness and selectivity of these chemicals, leading to more efficient and environmentally friendly agricultural practices.
Further research and experimentation are required to fully explore the properties and potential applications of [2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropyl]methyl acetate, as its complex structure and diverse functional groups offer numerous possibilities across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 81968-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81968-65:
(7*8)+(6*1)+(5*9)+(4*6)+(3*8)+(2*6)+(1*5)=172
172 % 10 = 2
So 81968-65-2 is a valid CAS Registry Number.
81968-65-2Relevant articles and documents
From Δ3-carene to the most biologically active insecticides: A convenient and efficient synthesis of (+)-(1R)-cis-chrysanthemic acid
Dhillon, Ranjit S,Gautam, Veena K,Singh, Swaranjit,Singh, Jasvinder
, p. 574 - 578 (2007/10/02)
A convenient and economical synthesis of (+)-(1R)-cis-chrysanthemic acid from Δ3-carene is reported.
Synthesis of Methyl 1R(+)-cis-Chrysanthemate and Methyl 1S(+)-cis-2,2-Dimethyl-3-(2-phenylprop-1-enyl)cyclopropane-1-carboxylate from (+)-Car-3-ene
Bhat, N. G.,Mane, B. M.,Kulkarni, G. H.,Mitra, R. B.
, p. 204 - 206 (2007/10/02)
Synthesis of (+)-dihydrochrysanthemolactone (III), methyl 1R(+)-cis-chrysanthemate (II) and methyl 1S(+)-cis-2,2-dimethyl-3-(2-phenylprop-1-enyl)cyclopropane-1-carboxylate (XIII) has been achieved from a common intermediate 2,2-dimethyl-3-(2-methyl-2-hydroxypropyl)-cis-1-acetonylcyclopropane (IV), which is obtainable from (+)-car-3-ene by a known procedure.
