950919-72-9 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-3-acetamido-3-phenylacrylic acid is used as a building block for the preparation of various pharmaceutical compounds and biologically active molecules. Its potential therapeutic properties, including anti-inflammatory and analgesic effects, make it an important target for drug discovery and development.
Used in Chemical Industry:
(Z)-3-acetamido-3-phenylacrylic acid is used as an intermediate in organic synthesis due to its unique molecular structure and reactivity. This allows for the creation of a wide range of complex organic molecules, contributing to the advancement of chemical research and product development.
Used in Research and Laboratory Settings:
Z-AAPA is utilized for its versatile chemical properties in research and laboratory settings. Its ability to serve as a valuable intermediate in the synthesis of complex organic molecules makes it a crucial component in scientific investigations and the development of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 950919-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,9,1 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 950919-72:
(8*9)+(7*5)+(6*0)+(5*9)+(4*1)+(3*9)+(2*7)+(1*2)=199
199 % 10 = 9
So 950919-72-9 is a valid CAS Registry Number.
950919-72-9Relevant academic research and scientific papers
Chen, Chunhui,Zhan, Ensheng,Li, Yong,Shen, Wenjie
, p. 117 - 121 (2013)
Enantioselective hydrogenation of (Z)-β-dehydroamino acids on a cinchonidine-modified Pd/Al2O3 catalyst was explored. Comparative studies by using (Z)-β-dehydroamino acids and esters identified that the carboxylic group in dehydroamino acids was essentially important to get enantioselectivities (33% for aryl substituted and 46% for alkyl substituted β-dehydroamino acids). This result extended the range of enantioselective hydrogenation of α,β-unsaturated carboxylic acids on chirally modified Pd catalysts and offered a new approach to synthesize optically active β-amino acids.
