3717-30-4

Upstream product

• 3717-29-1 E-3-nitrobenzaldoxime 
• 71-43-2 benzene 
• 5676-82-4 (3-nitrobenzylidene)aniline 
• 7803-49-8 hydroxylamine 
• 39089-86-6 3-nitro-benzaldehyde-(O-phenylcarbamoyl-seqcis-oxime ) 
• 99-61-6 3-nitro-benzaldehyde 
• 39089-86-6 3-nitro-benzaldehyde-(O-phenylcarbamoyl-seqtrans-oxime ) 
• 3848-31-5 3-nitro-benzaldehyde-((Z)-O-acetyl oxime ) 
• 62-53-3 aniline 
• 64-17-5 ethanol 

Downstream Products

• 33499-33-1 3-nitro-benzaldehyde-(O-methyl-seqcis-oxime ) 
• 16089-77-3 methyl-(3-nitro-benzylidene-(seqcis))-amine oxide 
• 619-24-9 3-nitrobenzonitrile 
• 3717-29-1 E-3-nitrobenzaldoxime 
• 2835-66-7 m-aminobenzaldehyde oxime 
• 74229-71-3 3,5-bis(3-nitrophenyl)-1,2,4-oxadiazole 
• 41401-08-5 bis-(3-nitro-benzylidene)-diazoxane-N-oxide 
• 99-61-6 3-nitro-benzaldehyde 
• 33512-94-6 m-nitrobenzhydroxamoyl chloride 
• 3848-31-5 3-nitro-benzaldehyde-((Z)-O-acetyl oxime ) 
• 13356-88-2 O-(2.4-dinitro-phenyl)-3-nitro-benz-anti-aldoxime 
• 33499-33-1 (E)-3-nitrobenzaldehyde O-methyloxime 
• 16089-77-3 N-methyl-α-(m-nitrophenyl)nitrone 
• 25387-14-8 3-hydroxy-2-(3-nitro-phenyl)-4-trichloromethyl-[1,3]oxazinan-6-one 

Relevant academic research and scientific papers

Host (dealuminated Y zeolite)–guest (zirconium tetraphenylporphyrin) nanocomposite materials. An efficient catalyst in the oximation of aldehydes

In this research, zirconium tetraphenylporphyrin encapsulated into dealuminated Y zeolite (ZrTPP–DAZY) was prepared through a template synthesis method. This heterogeneous catalyst was characterized by XRD, FT-IR, DRS, UV–Vis, EDX and FESEM techniques. The amount of ZrTPP in the nanocage of dealuminated Y zeolite was estimated to be 0.0156?g/g of support. This catalytic system was employed for an efficient oximation of aldehydes under magnetic stirring conditions at room temperature and the corresponding products were obtained in 50–90% yields. This catalytic system also indicated good shape selectivity towards linear aldehydes. ZrTPP–DAZY was reused several times without any significant loss in catalytic activity.

A facile steroselective synthesis of Z-aldoximes from benzaldehyde and hydroxlaminehydrochloride in dry media

The synthesis of Z-arylaldoximes has been carried out under microwave conditions using CdSO4 as catalyst. The yields obtained were in the range 84-88%.

Alumina sulfuric acid mediated solvent-free and one-step Beckmann rearrangement of ketones and aldehydes and a useful reagent for synthesis of keto- and ald-oximes

Under solvent-free conditions, one-step Beckmann rearrangement of a variety of ketones and aldehydes could proceed in the presence of alumina sulfuric acid (ASA). The ASA reagent can also be used for the preparation of keto- and ald-oximes.

Process for producing aminobenzylamines

Aminobenzylamines are produced by catalytically reducing o-, m- or p-nitrobenzaldoxime in an organic solvent in the presence of a compound selected from the group consisting of (a) boric acid, phosphoric acid and/or anhydrides thereof, (b) CO2 gas and (c) an organic acid. The starting material, nitrobenzaldoxime is produced by reaction of the corresponding nitrobenzaldehyde with hydroxylamine.