479064-93-2 Usage
Uses
Used in Pharmaceutical Industry:
Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure allows for the development of new drug candidates with improved pharmacological properties, such as enhanced potency, selectivity, and bioavailability.
Used in Peptide Synthesis:
In the field of peptide synthesis, Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid serves as a crucial building block for the creation of peptidomimetics. These are peptide-like compounds that mimic the structure and function of natural peptides but exhibit improved stability and bioavailability, making them attractive candidates for drug development.
Used in Medicinal Chemistry Research:
Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid is utilized as a versatile tool in medicinal chemistry research. Its unique structural features enable the exploration of novel chemical space and the design of new bioactive molecules with potential therapeutic applications.
Used in Drug Discovery:
In the drug discovery process, Boc-(R)-3-Amino-3-(4-chlorophenyl)propionic acid plays a significant role in the identification and optimization of lead compounds. Its incorporation into various chemical libraries allows for the screening of a wide range of potential drug candidates, accelerating the discovery of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 479064-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,0,6 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 479064-93:
(8*4)+(7*7)+(6*9)+(5*0)+(4*6)+(3*4)+(2*9)+(1*3)=192
192 % 10 = 2
So 479064-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H18ClNO4/c1-14(2,3)20-13(19)16-11(8-12(17)18)9-4-6-10(15)7-5-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1
479064-93-2Relevant academic research and scientific papers
α-Oxymethyl ketone enolates for the asymmetric Mannich reaction. From acetylene and N-alkoxycarbonylimines to β-amino acids
Palomo, Claudio,Oiarbide, Mikel,Gonzalez-Rego, M. Concepcion,Sharma, Arun K.,Garcia, Jesus M.,Gonzalez, Alberto,Landa, Cristina,Linden, Anthony
, p. 1063 - 1066 (2007/10/03)
The insufficient diastereoselectivity and generality, which are the main problems of the 'acetate' aza - aldol reaction, can now be addressed through the reaction of the lithium enolate of endo-O-trimethylsilyl acetyl isoborneol with various N[(p-tolylsul
