93103-00-5

Basic information

• Product Name: 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE
• Synonyms: 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE;3-α-aMinoacetylpyridine dihydrochloride;Ethanone, 2-aMino-1-(3-pyridinyl)-, hydrochloride
• CAS NO: 93103-00-5
• Molecular Formula: C₇H₈N₂O*2ClH
• Molecular Weight: 172.61
• Mol File: 93103-00-5.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE(93103-00-5)
• EPA Substance Registry System: 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE(93103-00-5)

Safety Data

• Hazardous Substances Data: 93103-00-5(Hazardous Substances Data)

Usage

General Description

2-Amino-1-pyridin-3-yl-ethanone hydrochloride is a chemical compound with the molecular formula C7H8ClN3O. It is a derivative of pyridine, and its hydrochloride salt form is a white crystalline solid. 2-AMINO-1-PYRIDIN-3-YL-ETHANONE HYDROCHLORIDE is commonly used in the pharmaceutical industry as an intermediate for the synthesis of various drug compounds. Its chemical structure and properties make it suitable for use in the preparation of different pharmaceutical products, particularly those targeting central nervous system disorders. Additionally, it has potential applications in research and development of new drugs and is an important building block in organic synthesis.

InChI:InChI=1/C7H8N2O.ClH/c8-4-7(10)6-2-1-3-9-5-6;/h1-3,5H,4,8H2;1H

Upstream product

• 5973-83-1 1-(pyridin-3-yl)ethan-1-one oxime 
• 98-59-9 p-toluenesulfonyl chloride 
• 74209-51-1 1-pyridin-3-yl-ethanone oxime O-tosylate 
• 626-55-1 3-Bromopyridine 
• 473693-42-4 tert-butyl (2-oxo-2-(pyridin-3-yl)ethyl)carbamate 
• 350-03-8 methyl-3-pyridylketone 
• 93102-88-6 5-Pyridin-3-yl-oxazole-4-carboxylic acid methyl ester 
• 6283-81-4 3-oxo-3-pyridin-3-yl-propionic acid ethyl ester 
• 92639-84-4 2-hydroxyimino-1-(3-pyridyl)-1-ethanone 
• 61296-12-6 2-hydroxyimino-3-oxo-3-[3]pyridyl-propionic acid ethyl ester 

Downstream Products

• 93103-29-8 4-(pyridin-3-yl)-1H-imidazole-2(3H)-thione 
• 51746-85-1 3-(1H-imidazol-4-yl)pyridine 
• 1233855-18-9 N-cyclohexyl-N-methyl-4-(pyridin-3-yl)-1H-imidazole-1-carboxamide 
• 1233855-46-3 3-(1-(cyclohexyl(methyl)carbamoyl)-1H-imidazol-4-yl)pyridine 1-oxide 
• 1356960-88-7 C₁₅H₁₁N₃O₂ 
• 1356960-60-5 N-benzyl-N-methyl-4-(pyridin-3-yl)-1H-imidazole-1-carboxamide 
• 93103-29-8 4-Pyridin-3-yl-1H-imidazole-2-thiol 
• 92990-44-8 2-amino-1-(pyridine-3-yl)ethanol 

Relevant articles and documents

COMPOUNDS USEFUL AS MODULATORS OF TRPM8

The present invention includes compounds useful as modulators of TRPM8, such as compounds of Formulae (Ia), (Ib) and (Ic), and the subgenus and species thereof; personal products containing those compounds; and the use of those compounds and the personal products, particularly the use of increasing or inducing chemesthetic sensations, such as cooling or cold sensations.

PROCESS FOR THE SYNTHESIS OF SUBSTITUTED UREA COMPOUNDS

A process for preparing a substituted urea compound of Formula II or Formula I, or a pharmaceutically acceptable salt or ester thereof, Formula II, Formula I the process comprising the reaction of an intermediate of Formula II' or Formula 1', Formula II',

NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS

Acetylcholine receptor ligands of formula (I), wherein D, Ar1, E and Ar2 are as described in the specification, diastereoisomers, enantiomers, pharmaceutically-acceptable salts, methods of making, pharmaceutical compositions containing and methods for usi