63304-82-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Methyl 2-(3-amino-4-methoxyphenyl)acetate is used as an intermediate in the synthesis of various pharmaceuticals for its potential pharmacological properties. Its unique structure allows it to be a key component in the creation of new drugs with specific therapeutic effects.
Used in Organic Chemistry:
In the field of organic chemistry, Methyl 2-(3-amino-4-methoxyphenyl)acetate is used as a building block for the synthesis of other organic compounds. Its versatile functional groups enable it to participate in a range of chemical reactions, contributing to the development of novel organic molecules with diverse applications.
Used in Research and Development:
Methyl 2-(3-amino-4-methoxyphenyl)acetate is utilized in research and development settings to explore its potential applications and properties. Scientists and researchers use Methyl 2-(3-amino-4-methoxyphenyl)acetate to investigate its interactions with biological systems, its reactivity in chemical reactions, and its potential use in creating new materials or drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 63304-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 63304-82:
(7*6)+(6*3)+(5*3)+(4*0)+(3*4)+(2*8)+(1*2)=105
105 % 10 = 5
So 63304-82-5 is a valid CAS Registry Number.
63304-82-5Relevant academic research and scientific papers
Efficient reducing system based on iron for conversion of nitroarenes to anilines
Xiao, Zhu-Ping,Wang, Ying-Chun,Du, Gao-Yu,Wu, Jun,Luo, Tao,Yi, Shou-Fu
experimental part, p. 661 - 665 (2011/03/19)
Reduction of nitroarenes with low solubility in EtOH-H2O to anilines easily occurs in a Fe-NH4Cl-acetone-H2O system, and treatment of the same nitroarenes with Fe-NH4Cl-EtOH-H2O hardly furnished the corresponding products. Under the reaction condition, the reducible or hydrolysable groups are not affected.
