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

• 79-24-3 Nitroethane 
• 555-16-8 4-nitrobenzaldehdye 
• 87-91-2 diethyl (2R,3R)-tartrate 
• 1129-37-9 4-nitrobenzaldoxime 
• 123-75-1 pyrrolidine 
• 75735-26-1 O-(2,4-dinitrophenyl)-p-nitrobenzaldoxime 
• 115828-63-2 4-nitro-benzaldehyde-(O-picryl-seqtrans-oxime ) 
• 590-28-3 potassium cyanate 
• 99-99-0 1-methyl-4-nitrobenzene 
• 110-89-4 piperidine 
• 58402-81-6 (Z)-4-nitrobenzohydroximoyl chloride 
• 54615-10-0 (E)-4-nitrobenzaldehyde O-methyl oxime 
• 7409-30-5 p-nitrobenzylamine 
• 619-73-8 4-nitrobenzyl chloride 

Downstream Products

• 41542-60-3 N-Hydroxy-4-nitro-thiobenzimidic acid 2-diethylamino-ethyl ester 
• 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 
• 54615-10-0 (E)-4-nitrobenzaldehyde O-methyl 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.

Poly(N-vinylimidazole): A biocompatible and biodegradable functional polymer, metal-free, and highly recyclable heterogeneous catalyst for the mechanochemical synthesis of oximes

The catalytic activity of poly(N-vinylimidazole), a biocompatible and biodegradable synthetic functional polymer, was investigated for the synthesis of oximes as an efficient, halogen-free, and reusable heterogeneous catalyst. The corresponding oximes were afforded in high to excellent yields at room temperature and in short times using the planetary ball mill technique. Some merits, such as the short reaction times and good yields for poorly active carbonyl compounds, and avoiding toxic, expensive, metal-containing catalysts, and hazardous and flammable solvents, can be mentioned for the current catalytic synthesis of the oximes. Furthermore, the heterogeneous organocatalyst could be easily separated after the reaction, and the regenerated catalyst was reused several times with no significant loss of its catalytic activity.