713513-03-2 Usage
Uses
Used in Pharmaceutical Industry:
(R)-3-Amino-3-(3,4-dimethoxy-phenyl)-propionic acid is used as a pharmaceutical intermediate for the development of drugs targeting neurological disorders and neurodegenerative diseases. Its unique structure and chirality allow for specific interactions with receptors in the central nervous system, potentially leading to more effective treatments for these conditions.
Used in Drug Research and Development:
(R)-3-Amino-3-(3,4-dimethoxy-phenyl)-propionic acid serves as a key molecule in drug research and development, particularly in the exploration of its interactions with central nervous system receptors. (R)-3-Amino-3-(3,4-dimethoxy-phenyl)-propionic acid's potential to modulate receptor activity and its chiral nature make it a valuable tool for understanding the mechanisms of neurological disorders and developing targeted therapies.
Used in Chiral Chemistry:
(R)-3-Amino-3-(3,4-dimethoxy-phenyl)-propionic acid is utilized in chiral chemistry for the synthesis of enantiomerically pure compounds. Its unique (R)-enantiomer form can be selectively incorporated into various chemical reactions, enabling the production of chiral molecules with specific biological activities and properties. This application is crucial in the development of enantiomerically pure drugs, which can exhibit improved efficacy and reduced side effects compared to their racemic counterparts.
Check Digit Verification of cas no
The CAS Registry Mumber 713513-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,3,5,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 713513-03:
(8*7)+(7*1)+(6*3)+(5*5)+(4*1)+(3*3)+(2*0)+(1*3)=122
122 % 10 = 2
So 713513-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4/c1-15-9-4-3-7(5-10(9)16-2)8(12)6-11(13)14/h3-5,8H,6,12H2,1-2H3,(H,13,14)/t8-/m1/s1
713513-03-2Relevant academic research and scientific papers
Kinetic resolution of aromatic β-amino acids by ω-transaminase
Bea, Han-Seop,Park, Hye-Jeong,Lee, Sang-Hyeup,Yun, Hyungdon
supporting information; experimental part, p. 5894 - 5896 (2011/06/23)
Racemic aromatic β-amino acids have been kinetically resolved into (R)-β-amino acids with high enantiomeric excess (>99%) by a novel ω-TA with ca. 50% conversion.
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.
