37961-71-0

Basic information

• Product Name: Benzaldehyde, 4-(dimethylamino)-, oxime, (E)-
• CAS NO: 37961-71-0
• Molecular Formula: C9H12N2O
• Molecular Weight: 164.207
• Mol File: 37961-71-0.mol
• Article Data: 47

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 4-(dimethylamino)-, oxime, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-(dimethylamino)-, oxime, (E)-(37961-71-0)
• EPA Substance Registry System: Benzaldehyde, 4-(dimethylamino)-, oxime, (E)-(37961-71-0)

Safety Data

• Hazardous Substances Data: 37961-71-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 127479-16-7 p-dimethylaminobenzaldehyde O-carbamoyloxime 
• 151-50-8 potassium cyanide 
• 19293-58-4 (4-aminomethylphenyl)dimethylamine 
• 100-10-7 4-dimethylamino-benzaldehyde 
• 590-28-3 potassium cyanate 
• 109-73-9 N-butylamine 
• 3986-36-5 4-dimethylamino-benzaldehyde-((E)-O-acetyl oxime ) 
• 1703-46-4 N,N-dimethyl-4-hydroxymethylaniline 
• 99-97-8 Dimethyl-p-toluidine 
• 7803-49-8 hydroxylamine 
• 4058-69-9 4-dimethylamino-benzaldehyde-(O-benzoyl oxime ) 
• 10050-89-2 4-dimethylamino-4'-(N,N-dimethylamino)benzylideneaniline 

Downstream Products

• 1197-19-9 4-cyano-N,N-dimethylaniline 
• 70405-05-9 C₁₆H₁₈N₄O 
• 54222-78-5 C₂₀H₂₈N₄O₂Si 
• 52629-36-4 O-Trimethylsilyl-p-dimethylaminobenzaldoxim 
• 19293-74-4 4-dimethylamino-benzaldehyde-(O-methyl oxime ) 
• 111530-18-8 3,4-bis(4-dimethylaminophenyl)-1,2,5-oxadiazole N-oxide 
• 6083-47-2 4-(dimethylamino)benzamide 
• 21530-39-2 C₁₁H₁₇N₃O 
• 57535-20-3 C₁₇H₂₂N₂OSi 
• 13181-86-7 4-dimethylamino-benzaldehyde-[O-(2,4-dinitro-phenyl)-oxime ] 
• 71063-92-8 4-dimethylamino-benzaldehyde-((E)-O-ethoxycarbonyl oxime ) 
• 19293-58-4 (4-aminomethylphenyl)dimethylamine 
• 100-10-7 4-dimethylamino-benzaldehyde 
• 7050-83-1 4-Dimethylamino-O-p-tolyloxycarbimidoyl-benzaldoxim 

Relevant articles and documents

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.

Effect of the Steric Hindrance and Branched Substituents on Visible Phenylamine Oxime Ester Photoinitiators: Photopolymerization Kinetics Investigation through Photo-DSC Experiments

In this work, free radical photopolymerization (FRP) kinetics for series of different phenylamine oxime ester structures (DMA–P, DEA–P, DMA–M, TP–2P, TP–2M and TP–3M) was investigated. Steric hindrance and branched substituents were prepared to realize th

Synthesis and biological evaluation of novel isoxazole derivatives from acridone

The present study was carried out in an?attempt to synthesize a new class of potential antibacterial agents. In this context, novel isoxazoles were synthesized and evaluated for their potential antibacterial behavior against four pathogenic bacterial strains. The synthesized compounds exhibited moderate-to-good antibacterial activity against these strains. The highest antibacterial activity was observed against the Escherichia coli strains, particularly for compounds 4a and 4e with phenyl and para-nitrophenyl groups on the isoxazole–acridone skeleton;?they showed promising minimum inhibitory concentration values of 16.88 and 19.01 μg/ml, respectively, compared with the standard drug chloramphenicol (22.41 μg/ml). The synthesized compounds were subjected to in silico docking studies to understand the mode of their interactions with the DNA topoisomerase complex (PDB ID: 3FV5) of E. coli. The molecular docking results showed that compounds 4a–l occupy the active site of DNA topoisomerase (PDB ID: 3FV5), stabilized via hydrogen bonding and hydrophobic interactions, which may be the reason behind their interesting in vitro antibacterial activity.