64757-64-8 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-AMINO-FURAN-2-YL-ACETIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its unique structural properties that can be exploited to create novel drug candidates.
Used in Biological Research:
(S)-AMINO-FURAN-2-YL-ACETIC ACID is used as a research compound for investigating its potential biological activities, which may lead to the discovery of new therapeutic applications.
Used in Material Science:
(S)-AMINO-FURAN-2-YL-ACETIC ACID is used as a building block in the development of new materials, taking advantage of its chemical reactivity and structural characteristics to create innovative compounds with specific properties.
Used in Organic Synthesis:
(S)-AMINO-FURAN-2-YL-ACETIC ACID is used as a versatile starting material in organic synthesis, allowing for the creation of a wide range of chemical products through various synthetic routes.
Check Digit Verification of cas no
The CAS Registry Mumber 64757-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,5 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64757-64:
(7*6)+(6*4)+(5*7)+(4*5)+(3*7)+(2*6)+(1*4)=158
158 % 10 = 8
So 64757-64-8 is a valid CAS Registry Number.
64757-64-8Relevant academic research and scientific papers
Asymmetric synthesis of arylglycines
Williams,Hendrix
, p. 3723 - 3727 (2007/10/02)
The asymmetric synthesis of several arylglycines are reported. The methodology deployed involves either cuprate or Friedel - Crafts couplings to chiral bromoglycinates. The % ee's range from 82 to 94%. Both an oxidative and reductive protocol are employed to unmask the oxazinone chiral auxilliary providing the free α-amino acids.
THE SYNTHESIS OF AMINO ACIDS BY REACTION OF AN ELECTROPHILIC GLYCINE CATION EQUIVALENT WITH NEUTRAL CARBON NUCLEOPHILES
O'Donell, Martin J.,Benett, William D.
, p. 5389 - 5402 (2007/10/02)
Seven neutral carbon nucleophiles (active aromatics, allylsilanes and a silyl enol ether) were reacted with the glycine cation equivalent 12 in the presence of TiCl4 to yield α-substituted amino acid derivatives in moderate yield (1-61.5 mmolar scale).Deprotection of the Schiff base ester products led to the corresponding amino acids.
