85367-01-7

Basic information

• Product Name: Benzamide, 3-nitro-N-2-pyridinyl-
• Synonyms: 3-nitro-N-(2-pyridinyl)benzamide;3-nitro-N-(pyridin-2-yl)benzamide
• CAS NO: 85367-01-7
• Molecular Formula: C₁₂H₉N₃O₃
• Molecular Weight: 243.22
• Mol File: 85367-01-7.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzamide, 3-nitro-N-2-pyridinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 3-nitro-N-2-pyridinyl-(85367-01-7)
• EPA Substance Registry System: Benzamide, 3-nitro-N-2-pyridinyl-(85367-01-7)

Safety Data

• Hazardous Substances Data: 85367-01-7(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 121-90-4 m-nitrobenzoic acid chloride 
• 1171753-50-6 N-tert-butyl-2-(3-nitrophenyl)imidazo[1,2-a]pyridin-3-amine 
• 99-61-6 3-nitro-benzaldehyde 
• 3034-94-4 3-nitrophenylacetylene 
• 4589-12-2 N-(pyrid-2-yl)benzamide 
• 5223-01-8 2-phenyl-N-(pyridin-2-yl)acetamide 
• 96354-74-4 N-(diphenylmethyl)pyridin-2-amine 
• 74037-48-2 N-(1,2-diphenylethyl)pyridin-2-amine 
• 923748-45-2 N-(pyridin-2-yl)monomethyl terephthalate monoamide 
• 121-92-6 3-nitrobenzoic acid 

Downstream Products

• 35005-25-5 m-isopropoxycarbonylaniline 
• 90234-15-4 C₁₄H₁₆N₄O₃S 
• 85367-02-8 3-amino-N-pyridin-2-yl-benzamide 

Relevant articles and documents

Diverse Oxidative C(sp2)-N Bond Cleavages of Aromatic Fused Imidazoles for Synthesis of α-Ketoamides and N-(pyridin-2-yl)arylamides

An efficient and chemoselective C(sp2)-N bond cleavage of aromatic imidazo[1,2-a]pyridine molecules is developed. A broad scope of amide compounds such as α-ketoamides and N-(pyridin-2-yl)arylamides are afforded as the final products in up to quantitative yields. Diverse C-N bond cleavages are controlled by the oxidative species used in this transformation, with various amide products afforded in a chemoselective fashion. A preliminary study indicated that some α-ketoamides exhibit anti-Tobacco Mosaic Virus activity for potential use in plant protection.

CuI incorporated cobalt ferrite nanoparticles as a magnetically separable catalyst for oxidative amidation reaction

A Cu-incorporated magnetic nanocatalyst (CoFe2O4?SiO2-SH-CuI) has been developed by immobilizing CuI on the modified surface of CoFe2O4 magnetic nanoparticles. The surface of the silica coated cobalt

AMINONAPTHOQUINONE COMPOUNDS AND PHARMACEUTICAL COMPOSITION FOR BLOCKING UBIQUITINATION-PROTEASOME SYSTEM IN DISEASES

The invention relates to new compounds with low cytotoxicity for blocking the ubiquitination- proteasome system in diseases. Accordingly, these compounds can be used in treatment of disorders including, but not limited to, cancers, neurodegenerative diseases, inflammatory disorders, autoimmune disorders and metabolic disorders.