5330-73-4

Basic information

• Product Name: 1-(4-nitrophenyl)-2-pyridin-1-yl-ethanone
• Synonyms: 1-[2-(4-Nitrophenyl)-2-oxoethyl]pyridinium; pyridinium, 1-[2-(4-nitrophenyl)-2-oxoethyl]-
• CAS NO: 5330-73-4
• Molecular Formula: C₁₃H₁₁N₂O₃*I
• Molecular Weight: 243.2375
• Mol File: 5330-73-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 1-(4-nitrophenyl)-2-pyridin-1-yl-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-nitrophenyl)-2-pyridin-1-yl-ethanone(5330-73-4)
• EPA Substance Registry System: 1-(4-nitrophenyl)-2-pyridin-1-yl-ethanone(5330-73-4)

Safety Data

• Hazardous Substances Data: 5330-73-4(Hazardous Substances Data)

Usage

Appearance

Yellow crystalline solid

Molecular weight

243.22 g/mol

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Application

Intermediate in the preparation of other organic compounds

Role

Reagent in chemical reactions

Structural feature

Different sources of media describe the Structural feature of 5330-73-4 differently. You can refer to the following data:
1. Presence of a nitro group
2. Presence of a pyridine ring

Utility

Useful for various applications in organic synthesis and medicinal chemistry

Potential

Further study and development in scientific and industrial fields

InChI:InChI=1/C13H11N2O3/c16-13(10-14-8-2-1-3-9-14)11-4-6-12(7-5-11)15(17)18/h1-9H,10H2/q+1

Upstream product

• 110-86-1 pyridine 
• 100-19-6 (4-nitrophenyl)ethanone 

Downstream Products

• 110186-76-0 methyl 2-(4-nitrophenyl)-2-oxoethanedithioate 
• 1514926-50-1 diethyl 3-(4-nitrobenzoyl)indolizine-1,2-dicarboxylate 
• 1234895-90-9 methyl 3-(p-nitrobenzoyl)indolizine-1-carboxylate 
• 1569317-73-2 12-(4-nitrobenzoyl)-5H-cyclohepta[1,2-b:3,4-b':5,6-b'']trinaphthalene-5,6,11,13,18,19(12H)-hexaone 
• 1325717-48-3 C₂₂H₁₄N₄O₄ 
• 943011-71-0 5-methyl-2-(4-nitrophenyl)pyridine 
• 112777-19-2 C₁₅H₁₂N₂O₃S₂ 
• 88007-99-2 2-methyl-3-(4-nitrophenacyl)-1,4-naphthoquinone 

Relevant articles and documents

Cyclization of Active Methylene Isocyanides with α-Oxodithioesters Induced by Base: An Expedient Synthesis of 4-Methylthio/Ethoxycarbonyl-5-acylthiazoles

Cyclization of tosylmethyl isocyanide with α-oxodithioesters in the presence of KOH is reported for the synthesis of 4-methylthio-5-acylthiazoles. Similarly, ethyl isocyanoacetate underwent cyclization with α-oxodithioesters to form 4-ethoxycarbonyl-5-acy

Kr?hnke pyridines: Rapid and facile access to Mcl-1 inhibitors

The tumorigenic activity of upregulated Mcl-1 is manifested by binding the BH3 α-helical death domains of opposing Bcl-2 family members, neutralizing them and preventing apoptosis. Accordingly, the development of Mcl-1 inhibitors largely focuses on synthe