1040-59-1 Usage
Uses
Used in Organic Synthesis:
(R)-3-(BENZYLOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is used as a key intermediate in organic synthesis for the creation of various complex molecules. Its unique structure allows for the development of novel compounds with potential applications in different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (R)-3-(BENZYLOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is used as a building block for the development of new drugs and medications. Its structural properties make it a promising candidate for the design of innovative therapeutic agents.
Used in Medicinal Chemistry:
(R)-3-(BENZYLOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is utilized in medicinal chemistry for the exploration of its potential biological activities. Its unique structure may contribute to the discovery of new therapeutic targets and the advancement of drug design strategies.
Used in Drug Design:
(R)-3-(BENZYLOXYCARBONYLAMINO)-2-PHENYLPROPANOIC ACID is also employed in drug design, where its structural features can be exploited to create new molecules with specific biological activities. This can lead to the development of more effective and targeted treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 1040-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1040-59:
(6*1)+(5*0)+(4*4)+(3*0)+(2*5)+(1*9)=41
41 % 10 = 1
So 1040-59-1 is a valid CAS Registry Number.
1040-59-1Relevant academic research and scientific papers
Enantioselective synthesis of 2-substituted 3-aminopropanoic acid (β-alanine) derivatives which are β-analogues of aromatic amino acids
Arvanitis, Elena,Ernst, Holger,Ludwig, Alice A.,Robinson, Andrew J.,Wyatt, Peter B.
, p. 521 - 528 (2007/10/03)
3-Aminopropanoic acid derivatives with a phenyl, 4-hydroxyphenyl, benzyl or indol-3-yl substituent at C-2 can be prepared enantioselectively by routes involving electrophilic attack of synthetic equivalents of [H2NCH2]+ upon enolates derived from chiral 3-acyl-1,3-oxazolidin-2-ones. tert-Butyl bromoacetate may be used as the electrophile, with subsequent introduction of nitrogen through the Curtius reaction, using the sequence of reagents (i) CF3CO2H; (ii) (PhO)2P(O)N3, Et3N, PhCH2OH; alternatively, direct electrophilic reaction with 1-[N-(benzyloxycarbonyl)aminomethyl]benzotriazole 4c or benzyl N-(acetoxymechyl)carbamate 2d introduces a protected aminomethyl group in a single step.
