40870-59-5

Usage

Uses

4-Methyl-3-nitrobenzyl alcohol may be used in chemical synthesis.

InChI:InChI=1/C8H9NO3/c1-6-2-3-7(5-10)4-8(6)9(11)12/h2-4,10H,5H2,1H3

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 10397-30-5 4-methyl-3-nitrobenzoyl chloride 
• 31680-07-6 4-methyl-3-nitrobenzaldehyde 

Downstream Products

• 81863-45-8 3-(hydroxymethyl)-6-methylaniline 
• 31680-07-6 4-methyl-3-nitrobenzaldehyde 
• 177164-94-2 5-[(hepta-O-acetyl-β-D-maltosyl)oxymethyl]-2-methy-1-nitrobenzene 
• 459450-38-5 5-(2-Piperidino-ethyl)-2-methyl-1H-indole-3-carboxylic acid 3-nitro-4-methyl-benzyl ester 
• 177165-02-5 5-(Tetra-O-acetyl-β-glucopyranosyloxymethyl)-2-methyl-1-nitrobenzene 
• 1416432-37-5 (4-methyl-3-nitrobenzyl)(phenyl)sulfane 
• 74101-71-6 2-Methyl-5-(-methyl)-nitrobenzol 
• 74101-73-8 2-Methyl-5-<β-(N'-acetyl-3',4'-dimethoxy-phenylethylamino)-methyl>-anilin 
• 74101-70-5 2-Methyl-5-<β-(3',4'-dimethoxy-phenylethylamino)-methyl>-nitrobenzol 
• 32989-68-7 trans-4-(β-dimethylaminovinyl)-3-nitrobenzaldehyde 
• 1075-26-9 6-(hydroxymethyl)indole 
• 1196-70-9 indole-6-carboxaldehyde 
• 751467-62-6 3-(3-dimethylamino-propyl)-2-(4-methyl-3-nitro-phenyl)-thiazolidin-4-one 
• 220178-63-2 3-(acetoxymethyl)-6-methyl-N-(acetyl)aniline 

Relevant academic research and scientific papers

HETEROARYL COMPOUNDS AS INHIBITORS OF PROGRAMMED NECROSIS PATHWAY, COMPOSITION AND METHOD USING THE SAME

The present disclosure provides heteroaryl compounds of Formula (I), processes for their preparation, pharmaceutical compositions containing them, and their use in the treatment of diseases and disorders, arising from or related to the programmed necrosis pathway.

Metal–Organic Framework-Encapsulated CoCu Nanoparticles for the Selective Transfer Hydrogenation of Nitrobenzaldehydes: Engineering Active Armor by the Half-Way Injection Method

A novel armor-type composite of metal–organic framework (MOF)-encapsulated CoCu nanoparticles with a Fe3O4 core (Fe3O4@SiO2-NH2-CoCu@UiO-66) has been designed and synthesized by the half-way injection method, which successfully serves as an efficient and recyclable catalyst for the selective transfer hydrogenation. In this half-way injection approach, the pre-synthetic Fe3O4@SiO2-NH2-CoCu was injected into the UiO-66 precursor solution halfway through the MOF budding period. The formed MOF armor could play a role of providing significant additional catalytic sites besides CoCu nanoparticles, protecting CoCu nanoparticles, and improving the catalyst stability, thus facilitating the selective transfer hydrogenation of nitrobenzaldehydes into corresponding nitrobenzyl alcohols in high selectivity (99 %) and conversion (99 %) rather than nitro group reduction products. Notably, this method achieves the precise assembly of a MOF-encapsulated composite, and the ingenious combination of MOF and nanoparticles exhibits excellent catalytic performance in the selective hydrogen transfer reaction, implementing a “1+1>2” strategy in catalysis.

INSECTICIDAL ARYL ISOXAZOLINE DERIVATIVES

The present invention relates to novel aryl isoxazoline derivatives having excellent insecticidal activity as insecticides and represented by the formula: and their use as insecticides and acarizides.