91130-39-1 Usage
Uses
Used in Pharmaceutical Industry:
Benzene, 4-cyclopropyl-1,2-diMethylis used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
This chemical compound is also utilized as a building block in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Polymer Production:
Benzene, 4-cyclopropyl-1,2-diMethylserves as a crucial component in the synthesis of polymers, which have a wide range of applications in various industries, including plastics, textiles, and coatings.
Used as a Solvent in Industrial Processes:
Due to its solvent properties, Benzene, 4-cyclopropyl-1,2-diMethylis employed in various industrial processes, aiding in the manufacturing and processing of different products.
Used in Medicinal Chemistry and Drug Discovery:
The unique structure and properties of Benzene, 4-cyclopropyl-1,2-diMethylmake it a promising candidate for medicinal chemistry and drug discovery, where it can be used to develop new compounds with potential therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 91130-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91130-39:
(7*9)+(6*1)+(5*1)+(4*3)+(3*0)+(2*3)+(1*9)=101
101 % 10 = 1
So 91130-39-1 is a valid CAS Registry Number.
91130-39-1Relevant academic research and scientific papers
Diels-Alder reactions for the construction of cyclopropylarenes
Arndt, Marion,Hilt, Gerhard,Khlebnikov, Alexander F.,Kozhushkov, Sergei I.,De Meijere, Armin
experimental part, p. 3112 - 3121 (2012/07/14)
The straightforward synthesis of new bicyclopropyl-substituted alkynes and 1,3-dienes and their application in cobalt-catalyzed Diels-Alder reactions are described. The cycloaddition processes generated the desired bicyclopropyl-substituted arene derivatives in moderate to good yields, depending on the steric congestion of the reaction partners. The regioselectivity of the cycloaddition was controlled by the ligand coordinated to the cobalt center. The cyclopropyl moiety remained unchanged over the course of the Diels-Alder reaction, indicating that no radical type intermediates were formed. Only in a single case did the DDQ oxidation of the primarily formed dihydroaromatic product lead to ring opening of a cyclopropyl subunit. In all of the other cases, cyclopropyl-modified arenes with various functionalities were obtained. Copyright
