51818-98-5

Basic information

• Product Name: N-(4-Formyl-2-nitrophenyl)acetamide
• Synonyms: N-(4-Formyl-2-nitrophenyl)acetamide;4'-Formyl-2'-nitroacetanilide
• CAS NO: 51818-98-5
• Molecular Formula: C₉H₈N₂O₄
• Molecular Weight: 208.17082
• Mol File: 51818-98-5.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 445.1°Cat760mmHg
• Flash Point: 223°C
• Appearance: /
• Density: 1.425g/cm³
• Vapor Pressure: 4.07E-08mmHg at 25°C
• Refractive Index: 1.658
• PKA: 13.35±0.70(Predicted)
• CAS DataBase Reference: N-(4-Formyl-2-nitrophenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Formyl-2-nitrophenyl)acetamide(51818-98-5)
• EPA Substance Registry System: N-(4-Formyl-2-nitrophenyl)acetamide(51818-98-5)

Safety Data

• Hazardous Substances Data: 51818-98-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H8N2O4/c1-6(13)10-8-3-2-7(5-12)4-9(8)11(14)15/h2-5H,1H3,(H,10,13)

Upstream product

• 1539-06-6 3-nitro-4-acetamidobenzoic acid 
• 73166-06-0 4-(hydroxymethyl)-2-nitroacetanilide 
• 7647-01-0 hydrogenchloride 
• 64818-14-0 1-acetylamino-4-diacetoxymethyl-2-nitro-benzene 
• 108-24-7 acetic anhydride 
• 122-85-0 para-acetamidobenzaldehyde 
• 64-19-7 acetic acid 
• 7664-93-9 sulfuric acid 

Downstream Products

• 78807-37-1 N-[4-(5-Methoxy-1H-benzoimidazol-2-yl)-2-nitro-phenyl]-acetamide 
• 3011-34-5 4-hydroxy-3-nitrobenzaldehyde 
• 51818-99-6 4-amino-3-nitro-benzaldehyde 
• 6393-40-4 4-Amino 3-nitro-benzonitrile 
• 871702-97-5 4-hydrazonomethyl-2-nitrophenylamine 
• 871702-96-4 4-amino-3-nitrobenzaldoxime 
• 713511-84-3 3-{2-[6-(4-tert-butyl-phenyl)-pyridin-2-yl]-1H-benzoimidazol-5-yl}-2-methyl-acrylic acid ethyl ester 

Relevant articles and documents

Agile Detection of Chemical Warfare Agents by Machine Vision: a Supramolecular Approach

The supramolecular detection by image analysis of a simulant chemical warfare agent on a solid device containing a selective molecular sensor based on a BODIPY scaffold is reported. The recognition properties were investigated in solution, demonstrating h

Design of a highly sensitive fluorescent probe for interfacial electron transfer on a TiO2 surface

Single-molecule fluorescent probe: The formation of the highly fluorescent 4-NHOH form of a 3,4-dinitrophenyl-substituted boron dipyrromethane dye can be used to study interfacial electron transfer on individual TiO2 particles (see picture; B yellow, C gray, F green, H white, O red). Kinetic and image analyses of the resulting fluorescence bursts reveal temporal dynamics of molecular interactions and reactive-site distributions.

FLUORESCENT PROBES

A compound represented by the formula (I) wherein R1 and R2 represent amino groups that substitute at adjacent positions on the benzene ring, wherein one of the amino groups may have one alkyl group; R3 and R4 r