36176-47-3

Usage

Appearance

Pale yellow solid

Solubility

Soluble in organic solvents

Uses

a. Building block for pharmaceutical and agrochemical products
b. Reagent in the synthesis of oxime ethers
c. Applications in pharmaceuticals, plastics, and agriculture

Properties

a. Antibacterial potential
b. Anticancer potential

Synthesis

Used in organic synthesis for the preparation of various products

Versatility

Valuable in the synthesis and development of new products for various industries

Upstream product

• 17333-79-8 p-methoxybenzenediazonium 
• 306-44-5 propanone 1-oxime 
• 122-84-9 4-methoxybenzyl methyl ketone 
• 110-46-3 isopentyl nitrite 
• 29865-49-4 2-nitro-1-(4-methoxylphenyl) propane 
• 121-97-1 4-Methoxypropiophenone 
• 141-97-9 ethyl acetoacetate 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 874-90-8 4-methoxybenzonitrile 
• 69849-48-5 N-(4-methoxyphenyl)-2-oxopropanamide 
• 100-09-4 4-methoxybenzoic acid 
• 1491163-09-7 (E,E)-2,5-bis[2-(2-quinolyl)ethenyl]-3,6-bis(4-methoxyphenyl)pyrazine 
• 124235-34-3 2,5-bis-methyl-3,6-bis-(4'-methoxyphenyl)-pyrazine 
• 1491163-19-9 3,6-bis(4-methoxyphenyl)pyrazine-2,5-dicarbaldehyde 
• 1491163-12-2 C₂₀H₂₂N₂O₂ 
• 1491163-06-4 (E,E)-2,5-bis{2-[4-(dipropylamino)phenyl]ethenyl}-3,6-bis(4-methoxyphenyl)pyrazine 
• 112626-33-2 1-(4-methoxyphenyl)-1,2-propanedione dioxime 
• 120869-05-8 N-[2-Hydroxy-1-(4-methoxy-phenyl)-propyl]-benzamide 
• 120869-01-4 N-[1-(4-Methoxy-phenyl)-2-oxo-propyl]-benzamide 

Relevant academic research and scientific papers

A novel oxidative reaction of 2-nitro-1-phenylpropane with sodium nitrite. A new approach to prepare 1-oximino-1-phenylacetones

A useful method for preparation of 1-oximino-1-phenylacetones via a novel oxidative reaction of 2-nitro-1-phenylpropanes with sodium nitrite was reported.

1,2,5-thiadiazole-2 oxide analogue and application thereof

The invention belongs to the field of pharmaceutical chemistry and discloses a 1,2,5-thiadiazole-2 oxide analogue and application thereof. The compound blocks a normal redox equilibrium process of schistosoma cells to kill schistosoma. When the drug conce

Diaryldistyrylpyrazines: Solvatochromic and acidochromic fluorophores

Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photop