134430-95-8 Usage
Description
[R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester, also known as (βS)-β-[[(1R)-1-Phenylethyl](phenylmethyl)amino]-4-(phenylmethoxy)-benzenepropanoic Acid Methyl Ester (CAS# 134430-95-8), is a complex organic compound with a light yellow oil appearance. It is characterized by its unique molecular structure, which includes phenylethyl, phenylmethyl, and phenylmethoxy groups, as well as a benzenepropanoic acid backbone. [R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester is valuable in the field of organic synthesis due to its versatile chemical properties and potential for further modification.
Uses
1. Used in Organic Synthesis:
[R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of reactions, such as substitution, addition, and rearrangement, making it a versatile building block for the development of new molecules with potential applications in various industries.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, [R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester is used as a starting material for the development of new drugs. Its structural diversity and reactivity make it an attractive candidate for the synthesis of novel therapeutic agents, particularly in the areas of pain management, inflammation, and other medical conditions.
3. Used in Chemical Research:
[R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester is also utilized in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic routes. Its unique structure provides researchers with valuable insights into the behavior of similar compounds and helps in the development of innovative synthetic strategies.
4. Used in Material Science:
In the field of material science, [R-(R,S)]-β-[(1-Phenylethyl)(phenylMethyl)aMino]-4-(phenylMethoxy)-benzenepropanoic Acid Methyl Ester can be used as a component in the development of new materials with specific properties, such as improved stability, enhanced reactivity, or unique optical characteristics. Its incorporation into polymers, for example, could lead to the creation of advanced materials with potential applications in various industries, including electronics, automotive, and aerospace.
Check Digit Verification of cas no
The CAS Registry Mumber 134430-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,4,3 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 134430-95:
(8*1)+(7*3)+(6*4)+(5*4)+(4*3)+(3*0)+(2*9)+(1*5)=108
108 % 10 = 8
So 134430-95-8 is a valid CAS Registry Number.
134430-95-8Relevant articles and documents
Homochiral lithium amides for the asymmetric synthesis of β-amino acids
Davies, Stephen G.,Garrido, Narciso M.,Kruchinin, Dennis,Ichihara, Osamu,Kotchie, Luke J.,Price, Paul D.,Mortimer, Anne J. Price,Russell, Angela J.,Smith, Andrew D.
, p. 1793 - 1811 (2007/10/03)
Secondary homochiral lithium amides derived from α-methylbenzylamine undergo highly diastereoselective conjugate additions to a range of α,β-unsaturated esters. The corresponding β-amino acids are readily liberated by successive N-debenzylation and ester hydrolysis, furnishing (R)-β-amino butyric acid, (R)-β-amino pentanoic acid, (S)-β-leucine, (R)-β-amino octanoic acid, (S)-β-phenylalanine, (S)-β-tyrosine methyl ether, (S)-β-tyrosine hydrochloride and (S)-β-(2-methoxyphenyl)-β-amino propanoic acid in high yields and high ee. The application of this procedure to the synthesis of the natural products (R)-β-DOPA and (R)-β-lysine is demonstrated. The development of a simplified one-pot reaction protocol applicable to the multi-gram scale synthesis of homochiral β-amino esters is also delineated.
