39658-45-2 Usage
Uses
Used in Pharmaceutical Synthesis:
6-Aminopyridine-3-acetic acid is utilized as a key building block in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs with potential therapeutic benefits.
Used in Neurological Treatments:
6-Aminopyridine-3-acetic acid is employed as a potential treatment for neurological disorders, specifically targeting conditions like multiple sclerosis and spinal cord injuries. Its ability to improve nerve conduction makes it a promising candidate for enhancing nerve function and regeneration, thereby offering potential relief and recovery for affected patients.
Used in Organic Chemistry:
In the field of organic chemistry, 6-Aminopyridine-3-acetic acid serves as a versatile intermediate, facilitating the creation of a range of organic compounds for diverse applications, from pharmaceuticals to specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 39658-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,5 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39658-45:
(7*3)+(6*9)+(5*6)+(4*5)+(3*8)+(2*4)+(1*5)=162
162 % 10 = 2
So 39658-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c8-6-2-1-5(4-9-6)3-7(10)11/h1-2,4H,3H2,(H2,8,9)(H,10,11)
39658-45-2Relevant academic research and scientific papers
Studies on 1,3-Benzoxazines. I. Synthesis of Primary 2-Amino-pyridines via the Reaction of Imidoyl Chlorides of 1,3-Benzoxazines with Pyridine N-Oxides
Wachi, Kazuyuki,Terada, Atsusuke
, p. 465 - 472 (2007/10/02)
A new synthetic method for primary 2-aminopyridine derivatives is described.Treatment of the imidoyl chlorides of 1,3-benzoxazines (1a-i) with pyridine N-oxides resulted in the introduction of an oxazine moiety into the α-position of the pyridine ring through rearrangement of the initially formed reaction adduct.Acid hydrolysis of the rearrangement products afforded 2-aminopyridine derivatives in excellent yields.When methoxypyridine N-oxides were used, products of a different type (10 and 14) were obtained.
