26148-38-9

Basic information

• Product Name: 1,2-Benzenediamine, N-2-pyridinyl-
• CAS NO: 26148-38-9
• Molecular Formula: C11H11N3
• Molecular Weight: 185.228
• Mol File: 26148-38-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1,2-Benzenediamine, N-2-pyridinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenediamine, N-2-pyridinyl-(26148-38-9)
• EPA Substance Registry System: 1,2-Benzenediamine, N-2-pyridinyl-(26148-38-9)

Safety Data

• Hazardous Substances Data: 26148-38-9(Hazardous Substances Data)

Usage

Classification

Aromatic amine

Physical state at room temperature

Dark grey to brown solid

Solubility in water

Sparingly soluble

Uses

Synthesis of pharmaceuticals, dyes, and other organic compounds

Potential applications

Anti-inflammatory and anti-cancer therapies

Health and environmental hazards

Considered hazardous to human health and the environment

Safety precautions

Proper safety measures should be taken when handling this compound

Upstream product

• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 25551-61-5 N-(2-nitrophenyl)-2-aminopyridine 
• 100-51-6 benzyl alcohol 
• 6631-37-4 2-(phenylamino)pyridine 
• 109-09-1 2-chloropyridine 
• 95-54-5 1,2-diamino-benzene 
• 504-29-0 2-aminopyridine 
• 609-73-4 o-nitroiodobenzene 

Downstream Products

• 244758-66-5 (E)-2-[2-(Cyclohexyl)ethenyl]-1-(2-pyridyl)-1H-benzimidazole 
• 132278-01-4 (E)-4,4-dimethyl-2-pentenoyl chloride 
• 244758-78-9 (Z)-2-(1-Fluoro-2-phenylethenyl)-1-(2-pyridyl)-1H-benzimidazole 
• 244758-61-0 (E)-1-(2-Pyridyl)-2-(4-methoxystyryl)-1H-benzimidazole 
• 371110-36-0 (E)-2-(3-Fluorostyryl)-1-(2-pyridyl)-1H-benzimidazole 
• 244758-68-7 (E)-2-[2-(2-Furyl)ethenyl]-1-(2-pyridyl)-1H-benzimidazole 
• 89659-87-0 1-methyl-3-(2-pyridyl)benzimidazolin-2-one 
• 89659-78-9 [2-(Pyridin-2-ylamino)-phenyl]-carbamic acid ethyl ester 

Relevant articles and documents

Double N,B-Type Bidentate Boryl Ligands Enabling a Highly Active Iridium Catalyst for C-H Borylation

Boryl ligands hold promise in catalysis due to their very high electron-donating property. In this communication double N,B-type boryl anions were designed as bidentate ligands to promote an sp2 C-H borylation reaction. A symmetric pyridine-con

The synthesis of benzimidazoles via a recycled palladium catalysed hydrogen transfer under mild conditions

An efficient synthesis of benzimidazoles was developed by virtue of a recycled palladium catalyzed hydrogen transfer. The reaction can be carried out smoothly under mild conditions to give rise to a variety of benzimidazoles with good to excellent yields. The palladium catalyst could be recovered easily and reused six times with great catalytic activity.

AGRICULTURAL CHEMICALS

The present invention relates to compounds which are of use in the field of agriculture as fungicides.