149597-91-1 Usage
Description
3,3-Diphenyl-D-alanine is an organic compound that is characterized by its white powder form. It is a derivative of D-alanine, an amino acid, with two phenyl groups attached to the third carbon. 3,3-Diphenyl-D-alanine is known for its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
3,3-Diphenyl-D-alanine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
3,3-Diphenyl-D-alanine is used as a reagent in the coupling of diphenylalanine with D-leucine Methyl ester. This process is essential for the creation of complex organic molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
Due to its unique chemical properties, 3,3-Diphenyl-D-alanine is also utilized in research and development for the study of peptide synthesis, protein structure, and the development of novel bioactive molecules. Its role in these studies contributes to the advancement of scientific knowledge and the discovery of new applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 149597-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,5,9 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 149597-91:
(8*1)+(7*4)+(6*9)+(5*5)+(4*9)+(3*7)+(2*9)+(1*1)=191
191 % 10 = 1
So 149597-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H15NO2/c16-14(15(17)18)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H,16H2,(H,17,18)/t14-/m1/s1
149597-91-1Relevant articles and documents
Synthesis of both enantiomers of β,β-diphenyl-α-alanine (Dip) from glycine using (S)- or (R)-2-[(N-benzylprolyl)amino] benzophenone as a reusable chiral auxiliary
Tararov, Vitali I.,Savel'eva, Tatyana F.,Kuznetsov, Nickolai Yu.,Ikonnikov, Nikolai S.,Orlova, Svetlana A.,Belokon', Yuri N.,North, Michael
, p. 79 - 83 (1997)
Preparative syntheses of enantiopure (S)- and (R)-Dip by α-C-alkylation with Ph2CHX (X=Cl or Br) of the glycine moiety in a Ni(II) Schiff's base complex 1 derived from glycine and (S)- or (R)-[(N-benzylprolyl)amino]benzophenone (BPB) is described. The diastereoselectivity of the alkylation with PhCH2Br in DMF in the presence of NaOH is both kinetically and thermodynamically controlled.
GADD45BETA TARGETING AGENTS
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, (2012/11/08)
Compounds based around tetrapeptide, tripeptide and dipeptide moeties and corresponding peptiod moeties. Related methods and pharmaceutical compositions for use in treatment of cancer, inflammatory diseases, and other disorders.
Process for the preparation of D(-) and L(+)-3,3-diphenylalanine and D(-) and L(+)-substituted 3,3-diphenylalanines and derivatives thereof
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, (2008/06/13)
A process for the preparation of D(-) and L(+)-3,3-diphenylalanine and D(-) and L(+)-substituted 3,3-diphenylalanines is described where N-protected DL-3,3-diphenylalanine or N-protected-DL-substituted 3,3-diphenylalanine are treated with (-)cinchonidine and the resulting salt resolved into the desired enantiomers, as well as derivatives thereof and valuable intermediates used in the process.
