3398-07-0

Basic information

• Product Name: 2-AMINOBENZALDEHYDE OXIME
• Synonyms: 2-AMINOBENZALDEHYDE OXIME
• CAS NO: 3398-07-0
• Molecular Formula: C₇H₈N₂O
• Molecular Weight: 136.15
• Mol File: 3398-07-0.mol
• Article Data: 6

Chemical Properties

• Melting Point: 134-135 °C
• Boiling Point: 276.2±23.0 °C(Predicted)
• Appearance: /
• Density: 1.18±0.1 g/cm3(Predicted)
• PKA: 10.98±0.10(Predicted)
• CAS DataBase Reference: 2-AMINOBENZALDEHYDE OXIME(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINOBENZALDEHYDE OXIME(3398-07-0)
• EPA Substance Registry System: 2-AMINOBENZALDEHYDE OXIME(3398-07-0)

Safety Data

• Hazardous Substances Data: 3398-07-0(Hazardous Substances Data)

Usage

Physical state

white to light yellow solid

Uses

chelating agent, particularly in metal ion removal and recovery processes

Ability

bind to metal ions, forming stable complexes

Applications

industrial and environmental applications, organic synthesis, production of pharmaceuticals

Studied properties

potential antioxidant and antimicrobial properties

Upstream product

• 271-58-9 anthranil 
• 6635-41-2 (Z)-2-nitrobenzaldehyde oxime 
• 7803-49-8 hydroxylamine 
• 64-17-5 ethanol 
• 5653-21-4 metazonic acid 
• 529-23-7 o-aminobenzaldehyde 
• 4836-00-4 (E)-2-nitrobenzaldehyde oxime 
• 25509-01-7 2-hydroxyamino-benzaldehyde-oxime 
• 552-89-6 2-nitro-benzaldehyde 
• 5344-90-1 2-Aminobenzyl alcohol 

Downstream Products

• 529-23-7 o-aminobenzaldehyde 
• 1885-29-6 anthranilic acid nitrile 
• 94963-92-5 2-benzoylamino-benzaldehyde-(O-benzoyl oxime ) 
• 75407-57-7 2-benzoylamino-benzaldehyde-oxime 
• 28181-30-8 4-ethoxy-3-phenyl-3,4-dihydro-1H-quinazoline-2-thione 
• 69906-01-0 2-ethylamino-benzaldehyde-oxime 
• 32907-43-0 quinazoline-N-oxide 
• 21642-45-5 2-(2-chloro-acetylamino)-benzaldehyde-oxime 
• 860192-63-8 4-ethoxy-3-o-tolyl-3,4-dihydro-1H-quinazoline-2-thione 
• 90878-20-9 2-amino-benzaldehyde-(O-methyl oxime ) 
• 32212-27-4 2-phenyl-1,2-dihydro-benzo[1,3,2]diazaborinine 3-oxide 

Relevant articles and documents

Eco-friendly H2O2 oxidation of 1,2-dihydroquinazoline-3-oxides to quinazoline-3-oxides

2-Aminobenzaldehyde, 1-(2-aminophenyl)ethanone, and 2-aminophenyl phenyl methanone oximes 1 were reacted with aromatic aldehydes to give the corresponding 1,2-dihydroquinazoline-3-oxides 2. The latter were converted in high yields to a series of quinazoli

An organocatalytic enantioselective direct α-heteroarylation of aldehydes with isoquinoline: N -oxides

A new protocol for the enantioselective direct α-heteroarylation of aldehydes with isoquinoline N-oxides, via chiral enamine catalysis, has been successfully developed. High enantiomeric excesses and moderate to good yields were achieved for a variety of α-heteroarylated aldehydes.

Studies on the reaction of quinazoline 3 oxide with ketone. The transformation of quinazoline 3 oxide into quinoline derivatives

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