51941-15-2

Basic information

• Product Name: Ethanone, 2-aMino-1-(3-pyridinyl)-
• Synonyms: Ethanone, 2-aMino-1-(3-pyridinyl)-;2-Amino-1-pyridin-3-yl-ethanone
• CAS NO: 51941-15-2
• Molecular Formula: C₇H₈N₂O
• Molecular Weight: 136.15122
• Mol File: 51941-15-2.mol

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C(protect from light)
• CAS DataBase Reference: Ethanone, 2-aMino-1-(3-pyridinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-aMino-1-(3-pyridinyl)-(51941-15-2)
• EPA Substance Registry System: Ethanone, 2-aMino-1-(3-pyridinyl)-(51941-15-2)

Safety Data

• Hazardous Substances Data: 51941-15-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
Ethanone, 2-amino-1-(3-pyridinyl)is used as a building block in the synthesis of pharmaceuticals for its ability to participate in a wide range of chemical reactions, contributing to the creation of diverse medicinal compounds.
Used in Agrochemical Development:
Similarly, in the agrochemical industry, Ethanone, 2-amino-1-(3-pyridinyl)serves as a key intermediate in the synthesis of various agrochemicals, aiding in the development of effective products for agricultural applications.
Used in Organic Synthesis:
Ethanone, 2-amino-1-(3-pyridinyl)is utilized as a versatile precursor in organic synthesis, taking advantage of its reactivity to form multiple types of chemical compounds for different applications.
Used in Drug Development:
Due to its unique structure, Ethanone, 2-amino-1-(3-pyridinyl)is also used in drug development, potentially leading to the creation of new therapeutic agents that can address unmet medical needs.

Upstream product

• 74209-51-1 1-pyridin-3-yl-ethanone oxime O-tosylate 
• 5973-83-1 1-(pyridin-3-yl)ethan-1-one oxime 
• 350-03-8 methyl-3-pyridylketone 

Downstream Products

• 93103-29-8 4-Pyridin-3-yl-1H-imidazole-2-thiol 
• 51746-85-1 3-(1H-imidazol-4-yl)pyridine 
• 173838-67-0 4-(3-pyridyl)-1H-imidazol-1-butanamide phthalimide 
• 128999-54-2 (3S,4S)-5-Cyclohexyl-3-hydroxy-4-[2-(8-propyl-6-pyridin-3-yl-[1,2,4]triazolo[4,3-a]pyrazin-3-yl)-3-pyridin-3-yl-propionylamino]-pentanoic acid [(S)-1-(3-aminomethyl-benzylcarbamoyl)-3-methyl-butyl]-amide 

Relevant articles and documents

Synthesis and Antibacterial Activity of Novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains

A series of novel 4″-O-desosaminyl clarithromycin derivatives with 11, 12-arylalkyl side chains was synthesized by coupling 6-deoxy-desosamine donors (18, 19) with 4″-OH of compounds 5a–c. The activities of the target compounds were tested against a series of macrolide-sensitive and macrolide-resistant pathogens. Some of them showed activities against macrolide sensitive and resistant pathogens, and compounds 21d and 21e displayed significant improvement of activities against resistant pathogens.