20602-89-5 Usage
Description
(2,2-Dimethyl-cyclopropyl)-essigsaeuremethylester, also known as methyl 2,2-dimethylcyclopropyl acetate, is a colorless liquid chemical compound with the molecular formula C9H16O2. It possesses a fruity odor and is known for its unique chemical properties.
Uses
Used in Flavoring Industry:
(2,2-Dimethyl-cyclopropyl)-essigsaeuremethylester is used as a flavoring agent in the food industry for its fruity odor, enhancing the taste and aroma of various food products.
Used in Organic Synthesis:
(2,2-Dimethyl-cyclopropyl)-essigsaeuremethylester serves as an intermediate in organic synthesis, contributing to the production of various chemical compounds and materials.
Used as a Solvent:
This chemical compound is also utilized as a solvent in different industrial processes, aiding in the dissolution and reaction of other substances.
Used in Research:
(2,2-Dimethyl-cyclopropyl)-essigsaeuremethylester has been studied for its potential pharmacological properties, such as antimicrobial and antioxidant effects, indicating its use in scientific research for developing new applications and understanding its properties further.
Check Digit Verification of cas no
The CAS Registry Mumber 20602-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20602-89:
(7*2)+(6*0)+(5*6)+(4*0)+(3*2)+(2*8)+(1*9)=75
75 % 10 = 5
So 20602-89-5 is a valid CAS Registry Number.
20602-89-5Relevant articles and documents
Mechanism and Synthetic Applications of the Photochemical Generation and X-H Insertion Reactions of Oxacarbenes
Pirrung, Michael C.,Chang, Virginia K.,DeAmicis, Carl V.
, p. 5824 - 5831 (2007/10/02)
A kinetic study of the photochemical ring expansion of cyclobutanones to oxacarbenes has shown that, in the presence of alcohol, the oxacarbene is generated irreversibly.Substrates for the intramolecular versions of the oxacarbene generation-insertion sequence (heteroalkylcyclobutanones) were prepared by an intramolecular -Baeyer-Villiger sequence.These have been used to form 5-, 6-, 7-, and 8-membered nitrogen, oxygen, and sulfur bicyclic ring systems.
