63753-10-6

Basic information

• Product Name: 5-nonylsalicylaldehyde
• Synonyms: 5-nonylsalicylaldehyde;2-Hydroxy-5-nonylbenzaldehyde
• CAS NO: 63753-10-6
• Molecular Formula: C₁₆H₂₄O₂
• Molecular Weight: 248.36056
• EINECS: 264-443-3
• Mol File: 63753-10-6.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 353.4°C at 760 mmHg
• Flash Point: 150.6°C
• Appearance: /
• Density: 1.001g/cm³
• Vapor Pressure: 1.76E-05mmHg at 25°C
• Refractive Index: 1.532
• CAS DataBase Reference: 5-nonylsalicylaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-nonylsalicylaldehyde(63753-10-6)
• EPA Substance Registry System: 5-nonylsalicylaldehyde(63753-10-6)

Safety Data

• Hazardous Substances Data: 63753-10-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H24O2/c1-2-3-4-5-6-7-8-9-14-10-11-16(18)15(12-14)13-17/h10-13,18H,2-9H2,1H3

Upstream product

• 104-40-5 4-Nonylphenol 
• 109-88-6 magnesium methanolate 
• 7664-93-9 sulfuric acid 
• 2414-98-4 magnesium ethylate 
• 100-97-0 hexamethylenetetramine 
• 67-56-1 methanol 
• 50-00-0 formaldehyd 
• 106-49-0 p-toluidine 
• 7757-83-7 sodium sulfite 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 252735-69-6 2-hydroxy-3-(morpholinomethyl)-5-nonylbenzaldehyde 
• 50849-47-3 5-nonyl-2-hydroxybenzaldehyde oxime 
• 1497456-56-0 2-allyloxy-5-nonyl-benzaldehyde 
• 1497456-74-2 2,3-dihydro-2-(2'-methoxy-5'-nonyl-phenyl)-4H-1-benzopyran-4-one 
• 1497456-78-6 2,3-dihydro-2-(2'-allyloxy-5'-nonyl-phenyl)-4H-1-benzopyran-4-one 
• 1497456-82-2 2,3-dihydro-2-(2'-methoxy-5'-nonyl-phenyl)-5-methoxy-4H-1-benzopyran-4-one 
• 1497456-51-5 2-methoxy-5-nonyl-benzaldehyde 
• 1074213-33-4 C₂₄H₄₀N₂O₂ 
• 919109-46-9 3-bromomethyl-5-nonyl-salicylaldehyde 
• 69048-55-1 2-hydroxy-3-nitro-5-nonylbenzaldehyde 

Relevant articles and documents

High-efficiency preparation method of long-chain alkyl salicylaldehyde (by machine translation)

The invention provides a preparation method: a long-chain alkyl salicylaldehyde. The long-chain alkyl phenol and paraformaldehyde react under the conditions of organic amine, magnesium salt, solvent and temperature and the like, and corresponding long-chain alkyl salicylaldehyde. The conversion rate of the 96% method is equal to or higher, the product separation is convenient, the used magnesium salt is usually industrial waste, the cost is low, and the method is convenient to recycle and recycle. The obtained compound is an organic intermediate with important application value, and plays an important application in the field of non-ferrous metal smelting and surface active agents and the like. (by machine translation)

Synthesis and antimicrobial screening of some novel chalcones and flavanones substituted with higher alkyl chains

As a part of our program to generate some novel flavonoid frameworks substituted with higher alkyl groups as possible antimicrobial agents, we have in total synthesized twelve novel chalcones (11-16) and their corresponding flavanones (17-22) substituted with either nonyl or dodecyl chains in ring B in very good to excellent yields. The synthesized compounds have been screened for their antimicrobial potential against six bacterial and four fungal strains. The tested compounds, in general, showed significant antibacterial and comparable antifungal activities. While the chalcone (16) with a dodecyl chain showed highly promising antibacterial activity against almost all the organisms tested, the chalcone (13) with nonyl chain showed promising antifungal activity against Candida rugosa and Aspergillus niger strains.

A NOVEL PROCESS FOR THE MANUFACTURE OF 5-NONYL SALICYLALDOXIME

The invention relates to a process for producing 5-nonyl salicylaldoxime that comprises of converting nonyl phenol to a 5-nonyl aldehyde in a two-step reaction using a novel catalyst mixture, followed by the oximation of the said aldehyde using hydroxylamine sulphate, and that the said catalytic process of aldehyde production is the main invention, in that the effective use of the catalyst mixture helps the reaction proceed at a faster and controlled rate which leads to a higher yield of aldehyde, as a result of complete conversion of all the reactants to the final products.