69-91-0 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Aminophenylacetic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structures of various drugs.
Used in Organic Chemistry:
As a building block in organic chemistry, 2-Aminophenylacetic acid is utilized in the creation of complex organic molecules and compounds.
Used in Urinary Tract Infections Treatment:
2-Aminophenylacetic acid has potential applications in the treatment of urinary tract infections, likely due to its ability to interact with biological systems and target the causative agents of such infections.
Used in Anti-Inflammatory and Analgesic Drug Development:
2-AMINOPHENYLACETIC ACID is also involved in the development of anti-inflammatory and analgesic drugs, potentially due to its influence on inflammatory pathways and pain perception mechanisms.
Used in the Production of Biologically Active Compounds:
Its chemical properties make 2-Aminophenylacetic acid an important component in the production of a variety of biologically active compounds, contributing to the development of new therapeutic agents and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 69-91-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 69-91:
(4*6)+(3*9)+(2*9)+(1*1)=70
70 % 10 = 0
So 69-91-0 is a valid CAS Registry Number.
InChI:InChI=1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)
69-91-0Relevant academic research and scientific papers
Optical Resolution by Preferential Crystallization of 1,1,3,3-Tetramethylbutylammonium Salt of N-Formyl-DL-α-phenylglycine
Shiraiwa, Tadashi,Miyazaki, Hideya,Imai, Tomoki,Sunami, Michio,Kurokawa, Hidemoto
, p. 661 - 666 (2007/10/02)
Infrared spectrum, solubility, and ternary phase diagram of solubility indicated that 1,1,3,3-tetramethylbutylammonium salt (DL-TMB salt) of N-formyl-DL-α-phenylglycine is a conglomerate.In order to resolve DL-TMB salt efficiently, crystallization of D- and L-TMB salts was examined by free energy of critical nucleation in supersaturated solutions.Successive preferential crystallization of DL-TMB salt was experimented at 10 deg C for racemic solution in ethanol with the degree of supersaturation of 130percent, and D- and L-α-phenylglycine with 100percent optical purity were obtained from pure D- and L-TMB salts.
STEREOSELECTIVE REDUCTION OF RACEMIC N-HYDROXYAMINO ACIDS BY OPTICALLY ACTIVE THIOLS-IRON(II)
Nambu, Yoko,Endo, Takeshi
, p. 999 - 1002 (2007/10/02)
Kinetic resolution of racemic N-hydroxyamino acids by the reduction with optically active thiols and a catalytic amount of ferrous ion gave optically active amino acids presumably through enantiodifferentiating coordination of substrates to thiol-Fe(II) complexes.
