744193-65-5 Usage
Uses
Used in Pharmaceutical Applications:
(R)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a key component in the development of new drugs and medications due to its unique chemical structure and potential therapeutic effects.
Used in Research:
(R)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is utilized in research settings to study its properties and explore its potential applications in various fields, including medicine and organic chemistry.
Used in Anti-inflammatory and Analgesic Applications:
(R)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as an anti-inflammatory and analgesic agent, leveraging its potential therapeutic properties to alleviate pain and reduce inflammation.
Used in Neurological Disorder Treatment:
(R)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID has been studied for its potential in treating neurological disorders, suggesting that it may have neuroprotective or disease-modifying effects.
Used as a Building Block in Organic Synthesis:
(R)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a building block for the synthesis of other organic compounds, highlighting its versatility and importance in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 744193-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,1,9 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 744193-65:
(8*7)+(7*4)+(6*4)+(5*1)+(4*9)+(3*3)+(2*6)+(1*5)=175
175 % 10 = 5
So 744193-65-5 is a valid CAS Registry Number.
744193-65-5Relevant academic research and scientific papers
Parallel synthesis of homochiral β-amino acids
Davies, Stephen G.,Mulvaney, Andrew W.,Russell, Angela J.,Smith, Andrew D.
, p. 1554 - 1566 (2008/02/09)
The parallel asymmetric synthesis of an array of 30 β-amino acids of high enantiomeric purity using the conjugate addition of homochiral lithium N-benzyl-N-(α-methylbenzyl)amide as the key step is accomplished. The experimental simplicity and highly practical nature of the protocol is demonstrated by the efficient parallel conversion of 15 α,β-unsaturated esters to both enantiomeric series of the corresponding β-amino acids in high overall yields and selectivities with minimal purification involved in each step of the reaction protocol.
