174848-02-3

Basic information

• Product Name: Benzaldehyde, 4-nitro-, oxime, radical ion(1-), (Z)- (9CI)
• Synonyms: Benzaldehyde, 4-nitro-, oxime, radical ion(1+), (Z)- (9CI)
• CAS NO: 174848-02-3
• Molecular Formula: C7H6N2O3
• Molecular Weight: 166.14
• Mol File: 174848-02-3.mol
• Article Data: 164

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzaldehyde, 4-nitro-, oxime, radical ion(1-), (Z)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-nitro-, oxime, radical ion(1-), (Z)- (9CI)(174848-02-3)
• EPA Substance Registry System: Benzaldehyde, 4-nitro-, oxime, radical ion(1-), (Z)- (9CI)(174848-02-3)

Safety Data

• Hazardous Substances Data: 174848-02-3(Hazardous Substances Data)

Upstream product

• 150246-34-7 C₆₃H₅NO 
• 159487-82-8 3-phenyl-[60]fullereno[1',2':4,5]isoxazoline 
• 155609-31-7 C₆₄H₅NO₃ 
• 555-16-8 4-nitrobenzaldehdye 
• 103-79-7 1-phenyl-acetone 
• 99-99-0 1-methyl-4-nitrobenzene 
• 110-46-3 isopentyl nitrite 
• 1028432-11-2 C₂₀H₂₈N₂O₅SSi 
• 619-73-8 4-nitrobenzyl chloride 
• 7409-30-5 p-nitrobenzylamine 
• 75735-26-1 O-(2,4-dinitrophenyl)-p-nitrobenzaldoxime 
• 74-89-5 methylamine 
• 108-91-8 cyclohexylamine 
• 108-03-2 1-Nitropropane 

Downstream Products

• 86120-19-6 O-benzyl oxime of 4-nitrobenzaldehyde 
• 52805-36-4 4-benzyloxybenzonitrile 
• 3065-06-3 O--4-nitro-benzaldoxim 
• 1464149-75-4 2,6-dimethyl-3,5-bis[3-(4-nitrophenyl)-5-trifluoromethylisoxazol-4-carbonyl]pyridine 
• 82076-00-4 3-[3-(4-Nitro-phenyl)-[1,2,4]oxadiazol-5-ylmethyl]-1H-indole 
• 3419-18-9 4-aminobenzaldehyde oxime 
• 22661-23-0 N-benzyl-4-nitro-isobenzaldoxime 
• 22661-28-5 N-(4-nitro-benzyl)-benzaldoxime 
• 86120-19-6 4-nitrobenzaldehyde O-benzyloxime 
• 5315-87-7 4-nitrobenzaldehyde semicarbazone 
• 22998-05-6 syn-4-Nitro-benzaldehyd-O--oxim 
• 22998-04-5 syn-4-Nitro-benzaldehyd-O--oxim 
• 65786-05-2 C₁₄H₁₀N₄O₆ 
• 50998-68-0 4-nitro-benzaldehyde-(O-allyl-seqtrans-oxime ) 

Relevant articles and documents

A catalytic regioselective procedure for the synthesis of aryl oximes in the presence of palladium nanoparticles

The synthesis of aryl oximes from aryl aldehyde derivatives was carried out using hydroxylamine hydrochloride and aluminum oxy hydroxide-supported palladium (Pd/AlO(OH) nanoparticles. The procedure is revealed via the regioselective synthesis of oxime der

Visible-Light-Mediated Strategies for the Preparation of Oxime Ethers Derived from O-H Insertions of Oximes into Aryldiazoacetates

Two visible-light-mediated O-H insertion protocols involving oximes and aryldiazoacetates leading to different products depending on the solvent employed are reported. In DCM, direct O-H insertion takes place. In THF, there is the additional incorporation of the ring-opened form of this solvent into the structure of the product. These metal-free protocols are mild and tolerant to air and moisture. The preparation of an acaricide has been developed as an example of synthetic application.

The local and natural sources in synthetic methods: the practical synthesis of aryl oximes from aryl aldehydes under catalyst-free conditions in mineral water

The synthesis of oximes from aryl aldehydes was prepared using hydroxylamine hydrochloride. The obtained oxime compounds were synthesized at maximum efficiency in mineral water at room temperature. The developed method is economical, practical and environmentally friendly. All of the aldehydes were converted the oxime a method using local sources and useful for industrial applications is introduced in the literature. Graphic abstract: In this study, addition elimination reaction, one of the important reactions of organic chemistry, was carried out using local sources. With this reaction, aryl oximes were obtained from aryl aldehydes in mineral water under catalyst-free conditions.[Figure not available: see fulltext.]