46133-07-7

Basic information

• Product Name: (E)-benzene-1,3-diylbis(N-hydroxymethanimine)
• CAS NO: 46133-07-7
• Molecular Formula: C₈H₈N₂O₂
• Molecular Weight: 164.1613
• Mol File: 46133-07-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 315.814°C at 760 mmHg
• Flash Point: 192.292°C
• Density: 1.2g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: (E)-benzene-1,3-diylbis(N-hydroxymethanimine)(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-benzene-1,3-diylbis(N-hydroxymethanimine)(46133-07-7)
• EPA Substance Registry System: (E)-benzene-1,3-diylbis(N-hydroxymethanimine)(46133-07-7)

Safety Data

• Hazardous Substances Data: 46133-07-7(Hazardous Substances Data)

Usage

General Description

(E)-benzene-1,3-diylbis(N-hydroxymethanimine) is a chemical compound with the molecular formula C14H14N2O2. It is an organic compound comprised of a benzene ring with two N-hydroxymethanimine groups attached in a para position. (E)-benzene-1,3-diylbis(N-hydroxymethanimine) is commonly used in the preparation of various coordination compounds and metal complexes due to its ability to act as a bidentate ligand. It is also used in the synthesis of organic dyes and pigments. Additionally, (E)-benzene-1,3-diylbis(N-hydroxymethanimine) has potential applications in the field of medicinal chemistry, particularly in the development of new drugs and pharmaceuticals. Overall, this chemical compound has various uses and applications in different industries.

Upstream product

• 540-80-7 tert.-butylnitrite 
• 12129-28-1 (η6-m-xylene)tricarbonylchromium(0) 
• 52108-21-1 3-((hydroxyimino)methyl)benzaldehyde 
• 626-19-7 Isophthalaldehyde 

Downstream Products

• 18728-47-7 N,N-dihydroxybenzene-1,3-dicarboximidoyl dichloride 
• 626-17-5 benzene-1,3-dicarbonitrile 
• 7732-18-5 water 
• 3248-41-7 isophthalonitrile N,N'-dioxide 
• 3441-01-8 3-cyanobenzamide 
• 3030-54-4 1,3-benzenedicarboxylic acid dithioamide 
• 287398-41-8 C₂₄H₄₀N₂O₄Si₄ 

Relevant articles and documents

BSA nanoparticles as controlled release carriers for isophethalaldoxime palladacycle complex; Synthesis, characterization,: In vitro evaluation, cytotoxicity and release kinetics analysis

A new oxime ligand named isophthalaldoxime (1) was synthesized by the addition of hydroxylamine hydrochloride to isophthalaldehyde. Then, a four nuclear palladacycle complex {Pd4[(N,C)(NOHCHC6H2CHNOH)(μ-Cl)2]su

Novel isoxazoline ligand with ferrocene backbone: Preparation and application in Heck reaction with water as solvent

Two novel isoxazoline N,N-bidentate ligands with ferrocene backbone have been synthesized and employed for the palladium-catalyzed Heck coupling reaction. Among them, 1,3-bis-(5-ferrocenylisoxazoline-3-yl)benzene was found to be thermally stable and a highly effective ligand for Heck coupling reaction in neat water without N2 protection, affording the desired coupling products in good to excellent yield with high diastereoselectivity. The developed catalytic system was also well workable for 1,2-disubstituted alkenes, which were less involved in the Heck reaction for its larger steric hindrance. Copyright

Synthesis of isoxazoles by hypervalent iodine-induced cycloaddition of nitrile oxides to alkynes

Treatment of oximes with hypervalent iodine leads to substituted isoxazoles via rapid formation of nitrile oxides. Reaction with terminal alkynes led to a series of 3,5-disubstituted isoxazoles with complete regioselectivity and high yield, in a procedure