110853-58-2

Basic information

• Product Name: Benzaldehyde, 2,4-dichloro-, oxime, (E)-
• CAS NO: 110853-58-2
• Molecular Formula: C7H5Cl2NO
• Molecular Weight: 190.029
• Mol File: 110853-58-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2,4-dichloro-, oxime, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2,4-dichloro-, oxime, (E)-(110853-58-2)
• EPA Substance Registry System: Benzaldehyde, 2,4-dichloro-, oxime, (E)-(110853-58-2)

Safety Data

• Hazardous Substances Data: 110853-58-2(Hazardous Substances Data)

Upstream product

• 95-00-1 2,4-dichloro-benzenemethanamine 
• 874-42-0 2,4-dichlorobenzaldeyhde 

Downstream Products

• 50-84-0 2,4 dichlorobenzoic acid 
• 6574-98-7 2,4-dichlorobenzylnitrile 
• 69792-78-5 5-methyl-3-(2,4-dichlorophenyl)-1,2,4-oxadiazole 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 121197-64-6 3-(2,4-dichlorophenyl)-2-(diphenylphosphinoyl)oxaziridine 
• 208844-74-0 3-[1-(2,4-Dichloro-phenyl)-meth-(E)-ylideneaminooxy]-propionic acid hydrazide 
• 54696-53-6 3,4-di-(2,4-dichlorophenyl)furoxan 
• 121197-54-4 C₁₉H₁₄Cl₂NOP 

Relevant articles and documents

3-methyl-4-oxa-5-azahomoadamantane as an organocatalyst for the aerobic oxidation of primary amines to oximes in water

A simple and efficient catalytic system for the aerobic oxidation of primary amines into corresponding oximes has been developed, with 3-methyl-4-oxa-5-azahomoadamantane as catalyst, acetaldoxime as co-catalyst and water as solvent. This process, which uses oxygen (O2) as an economic and green oxidant and water as a green solvent, tolerates a wide range of substrates, affording the target oximes in moderate to excellent yields. It was found that high selectivity was achieved when 3-methyl-4-oxa-5-azahomoadamantane was used, and E-type oximes were the only detected products. A possible mechanism for this catalytic process is proposed.

A novel and efficient catalytic system including TEMPO/acetaldoxime/InCl3 for aerobic oxidation of primary amines to oximes

A simple and efficient catalytic system including TEMPO/acetaldoxime/InCl3 for aerobic oxidation of primary amines to corresponding oximes by using toluene as the solvent is described. This practical method can use O2 as the economic and green oxidant, tolerate a wide range of substrates, which can afford the target oximes in moderate to excellent yields.

BIFUNCTIONAL HETEROCYCLIC COMPOUNDS AND METHODS OF MAKING AND USING SAME

The invention provides a family of bifunctional heterocyclic compounds useful as anti-infective, anti-proliferative, anti-inflammatory, and prokinetic agents. The invention also provides methods of making the bifunctional hetercyclic compounds, and methods of using such compounds as anti-infective, anti-proliferative agents, anti-inflammatory, and/or prokinetic agents.