59084-78-5 Usage
Uses
Used in Organic Synthesis:
6-Cyano-2,3-dimethoxy-benzoic acid methyl ester is used as a building block in the synthesis of more complex organic compounds, contributing to the development of novel chemical entities with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 6-Cyano-2,3-dimethoxy-benzoic acid methyl ester is used as a key intermediate in the development of new drugs and pharmaceutical products. Its unique chemical structure allows for the exploration of its potential therapeutic effects and incorporation into medicinal formulations.
Used in Drug Development:
6-Cyano-2,3-dimethoxy-benzoic acid methyl ester is employed in drug development for its potential applications in creating new therapeutic agents. Its chemical properties make it a promising candidate for further research and development in medicinal chemistry.
Overall, 6-Cyano-2,3-dimethoxy-benzoic acid methyl ester is a significant chemical compound with a broad range of potential applications across different industries, particularly in the fields of organic synthesis and pharmaceutical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 59084-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,8 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59084-78:
(7*5)+(6*9)+(5*0)+(4*8)+(3*4)+(2*7)+(1*8)=155
155 % 10 = 5
So 59084-78-5 is a valid CAS Registry Number.
59084-78-5Relevant academic research and scientific papers
Asymmetric synthesis of 3-substituted isoindolinones: Application to the total synthesis of (+)-lennoxamine
Comins, Daniel L.,Schilling, Stefan,Zhang, Yanchen
, p. 95 - 98 (2007/10/03)
(Chemical Equation Presented) An anionic chiral auxiliary mediated asymmetric alkylation of carbamate 2 provides 3-substituted isoindolinones 4 in high ee. This methodology was used in the first asymmetric synthesis of (+)-lennoxamine.
