35202-54-1 Usage
Description
4,5-Dimethoxy-1-cyanobenzocyclobutane is an organic compound characterized by its unique molecular structure, which features a benzene ring fused to a cyclobutane ring, with a cyano group and two methoxy groups attached. 4,5-Dimethoxy-1-cyanobenzocyclobutane is known for its potential applications in the pharmaceutical and chemical industries due to its specific functional groups and structural properties.
Uses
Used in Pharmaceutical Industry:
4,5-Dimethoxy-1-cyanobenzocyclobutane is used as a key intermediate in the synthesis of selective bradycardic agents. These agents are designed to slow down the heart rate, which can be beneficial in treating conditions like tachycardia and certain arrhythmias. 4,5-Dimethoxy-1-cyanobenzocyclobutane's structural features allow for the development of targeted therapies with minimal side effects.
Additionally, 4,5-Dimethoxy-1-benzocyclobutenecarbonitrile, a related compound, is also used in the preparation of selective bradycardic agents. This highlights the versatility and importance of the benzocyclobutane framework in the development of cardiovascular medications.
Check Digit Verification of cas no
The CAS Registry Mumber 35202-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,0 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35202-54:
(7*3)+(6*5)+(5*2)+(4*0)+(3*2)+(2*5)+(1*4)=81
81 % 10 = 1
So 35202-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO2/c1-13-10-4-7-3-8(6-12)9(7)5-11(10)14-2/h4-5,8H,3H2,1-2H3
35202-54-1Relevant articles and documents
Process for the enzymatic synthesis of (7S)-3,4-dimethoxybicyclo[4.2.0]OCTA-1,3,5-triene-7-carboxylic acid and application in the synthesis of ivabradine and salts thereof
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Page/Page column 8, (2016/11/14)
Process for the enzymatic synthesis of the compound of formula (I): comprising enantioselective enzymatic hydrolysis of the nitrile of formula (IV): using the nitrilase of Rhodococcus rhodochrous of EMBL accession number EF467367.1, and the application of such a process in the synthesis of ivabradine and addition salts thereof with a pharmaceutically acceptable acid.
PROCESS FOR THE SYNTHESIS OF 3-(2-BROMO-4,5-DIMETHOXYPHENYL)PROPANENITRILE, AND APPLICATION IN THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID
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, (2014/06/24)
Process for the synthesis of the compound of formula (I): Application in the synthesis of ivabradine, addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof.
PROCESS FOR THE SYNTHESIS OF 3-(2-BROMO-4,5-DIMETHOXYPHENYL)PROPANENITRILE, AND APPLICATION IN THE SYNTHESIS OF IVABRADINE AND ADDITION SALTS THEREOF WITH A PHARMACEUTICALLY ACCEPTABLE ACID
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, (2014/05/07)
Process for the synthesis of the compound of formula (I): Application in the synthesis of ivabradine, addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof.