91702-86-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Pyridinecarboxylic acid, 5-(methylamino)-, methyl ester is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure and reactivity.
Used in Agrochemical Industry:
3-Pyridinecarboxylic acid, 5-(methylamino)-, methyl ester is used as a building block for the synthesis of agrochemicals, contributing to the development of effective crop protection agents.
Used in Antituberculosis Drug Preparation:
3-Pyridinecarboxylic acid, 5-(methylamino)-, methyl ester is used as a precursor in the preparation of antituberculosis agents such as ethambutol, playing a crucial role in the development of treatments for tuberculosis.
Used in Medical Research:
Nicotinamide methylate is used in research for its potential role in the treatment of various medical conditions, including diabetes and neurodegenerative diseases, due to its unique chemical properties and biological activity.
Used in Vitamin B3 Supplement Production:
3-Pyridinecarboxylic acid, 5-(methylamino)-, methyl ester is utilized in the production of vitamin B3 supplements, contributing to the development of nutritional supplements that support overall health and well-being.
Used in Drug Therapy Development:
Nicotinamide methylate is being investigated for its potential use in the development of new drug therapies, as its unique properties and biological activity offer promising avenues for the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 91702-86-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,0 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91702-86:
(7*9)+(6*1)+(5*7)+(4*0)+(3*2)+(2*8)+(1*6)=132
132 % 10 = 2
So 91702-86-2 is a valid CAS Registry Number.
91702-86-2Relevant academic research and scientific papers
Convenient synthesis of aminopyridinecarboxylic acids
Okamoto, Iwao,Terashima, Masayuki,Yoshioka, Rempei,Muramatsu, Tomonori,Kojima, Satomi,Inoue, Haruka,Takahashi, Mio,Morita, Nobuyoshi,Tamura, Osamu
experimental part, p. 2343 - 2352 (2011/11/06)
6-(Alkylamino)pyridine-2-carboxylic acids and 5-(alkylamino)pyridine-3- carboxylic acids were conveniently synthesized from dibromopyridine in satisfactory yields.
DERIVATIVES OF AMINOPYRIDINECARBOXYLIC ACIDS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
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, (2008/06/13)
Derivatives of aminopyridinecarboxylic acids which inhibit the dipeptidyl carboxy peptidase (DPCP), methods for their preparation and pharmaceutical compositions containing them.The compounds have formula: STR1 where Z is hydrogen, alkyl having from 1 to 3 carbon atoms, halogen or alkoxy having from 1 to 3 carbon atoms;R1 is hydrogen, alkyl having from 1 to 6 carbon atoms, arylalkyl having from 7 to 12 carbon atoms, aryl having from 6 to 15 carbon atoms;m and n are an integer of from 0 to 4 each provided, however, the m+n is lower than 5;R2 is hydrogen, alkyl having from 1 to 6 carbon atoms or arylalkyl having from 7 to 12 carbon atoms;R3 is hydrogen or acyl having from 1 to 8 carbon atoms;R4 is hydrogen or alkyl having from 1 to 3 carbon atoms;and their pharmaceutically acceptable salts with organic or inorganic acids.
