17119-54-9 Usage
Uses
Used in Pharmaceutical Industry:
AMINO-FURAN-2-YL-ACETIC ACID is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Organic Chemistry Research:
AMINO-FURAN-2-YL-ACETIC ACID is used as a research compound for the development of new synthetic methods in organic chemistry, contributing to the advancement of chemical synthesis techniques.
Used in Anti-Inflammatory Applications:
AMINO-FURAN-2-YL-ACETIC ACID is used as a potential therapeutic agent for its anti-inflammatory properties, offering a promising avenue for the treatment of inflammation-related conditions.
Used in Drug Development:
AMINO-FURAN-2-YL-ACETIC ACID is used in the development of new drugs, leveraging its potential therapeutic properties and chemical versatility to create innovative pharmaceutical formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 17119-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,1 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17119-54:
(7*1)+(6*7)+(5*1)+(4*1)+(3*9)+(2*5)+(1*4)=99
99 % 10 = 9
So 17119-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO3/c7-5(6(8)9)4-2-1-3-10-4/h1-3,5H,7H2,(H,8,9)
17119-54-9Relevant academic research and scientific papers
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.
