27696-01-1 Usage
Uses
Used in Pharmaceutical Industry:
N-BENZOYL-L-THREONINE is used as a chiral building block for the synthesis of peptides and pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Industry:
N-BENZOYL-L-THREONINE is used as a chiral ligand in asymmetric catalysis, facilitating the production of enantiomerically pure compounds for various applications.
Used in Research and Development:
N-BENZOYL-L-THREONINE is used as a research compound for studying its potential anti-inflammatory and anti-cancer properties, aiding in the discovery of novel therapeutic agents.
Used in Organic Synthesis:
N-BENZOYL-L-THREONINE is used as a versatile chemical intermediate in various organic synthesis processes, enabling the creation of a wide range of chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 27696-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27696-01:
(7*2)+(6*7)+(5*6)+(4*9)+(3*6)+(2*0)+(1*1)=141
141 % 10 = 1
So 27696-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-7(13)9(11(15)16)12-10(14)8-5-3-2-4-6-8/h2-7,9,13H,1H3,(H,12,14)(H,15,16)/t7-,9+/m1/s1
27696-01-1Relevant academic research and scientific papers
Reactivity of α-Amino Acids in the Reaction with Esters in Aqueous–1,4-Dioxane Media
Kochetova,Kustova,Kuritsyn
, p. 80 - 85 (2018/03/09)
The kinetics of the reaction of a series of α-amino acids with 4-nitrophenyl acetate, 4-nitrophenyl benzoate, and 2,4,6-trinitrophenyl benzoate in aqueous 1,4-dioxane medium has been studied. Kinetics of the reactions involving 4-nitrophenyl acetate and 2,4,6-trinitrophenyl benzoate has complied with the Br?nsted dependence and revealed linear correlation between rate constant logarithm and the energy difference of the frontier orbitals of α-amino acids anions.
Resolution of β-hydroxy-α-amino acids by the action of proteases on their N-acyl methyl esters
Chenevert, Robert,Letourneau, Martin,Thiboutot, Sonia
, p. 960 - 963 (2007/10/02)
Methyl N-acetyl phenylserinates (1, 2), methyl N-acetyl nitrophenylserinates (3, 4), and methyl N-benzoyl threoninates (5, 6) were resolved conveniently into the enantiomers with high optical purities by enzymatic hydrolysis in the presence of α-chymotryp
