93972-06-6

Basic information

• Product Name: 4-(4-N-BUTYLPHENYL)BENZALDEHYDE
• Synonyms: 4-(4-N-BUTYLPHENYL)BENZALDEHYDE
• CAS NO: 93972-06-6
• Molecular Formula: C17H18O
• Molecular Weight: 238.32
• Mol File: 93972-06-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(4-N-BUTYLPHENYL)BENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-N-BUTYLPHENYL)BENZALDEHYDE(93972-06-6)
• EPA Substance Registry System: 4-(4-N-BUTYLPHENYL)BENZALDEHYDE(93972-06-6)

Safety Data

• Hazardous Substances Data: 93972-06-6(Hazardous Substances Data)

Usage

General Description

4-(4-N-butylphenyl)benzaldehyde is a chemical compound that belongs to the class of benzaldehyde derivatives. It is an aromatic compound with a benzene ring substituted with a butyl group and a benzaldehyde functional group. 4-(4-N-BUTYLPHENYL)BENZALDEHYDE has potential applications in the field of organic synthesis and chemical research due to its unique structure and reactivity. It can also serve as a building block for the synthesis of more complex organic compounds and pharmaceutical products. However, its specific properties and potential uses may vary depending on the context and application.

Upstream product

• 52709-83-8 4'-n-butyl-4-cyanobiphenyl 
• 5720-05-8 4-methylphenylboronic acid 
• 1122-91-4 4-bromo-benzaldehyde 
• 145240-28-4 4-butylphenylboronic acid 
• 41492-05-1 p-bromobutylbenzene 
• 87199-17-5 4-formylphenylboronic acid, 
• 93972-13-5 4'-Butyl-biphenyl-4-carbaldehyde oxime 
• 13211-01-3 1-([1,1'-biphenyl]-4-yl)butan-1-one 
• 37909-95-8 4-butylbiphenyl 
• 92-52-4 biphenyl 

Downstream Products

• 1451207-36-5 C₃₈H₄₂N₂O₄ 
• 1451207-37-6 C₄₃H₅₀N₂O₆ 
• 1451207-42-3 C₄₂H₄₈N₂O₆ 

Relevant articles and documents

Gold Catalysts Can Generate Nitrone Intermediates from a Nitrosoarene/Alkene Mixture, Enabling Two Distinct Catalytic Reactions: A Nitroso-Activated Cycloheptatriene/Benzylidene Rearrangement

Gold-catalyzed reactions of cycloheptatrienes with nitrosoarenes yield nitrone derivatives efficiently. This reaction sequence enables us to develop gold-catalyzed aerobic oxidations of cycloheptatrienes to afford benzaldehyde derivatives using CuCl and nitrosoarenes as co-catalysts (10-30 mol %). Our density functional theory calculations support a novel nitroso-activated rearrangement, tropylium → benzylidene. With the same nitrosoarenes, we developed their gold-catalyzed [2 + 2 + 1]-annulations between nitrosobenzene and two enol ethers to yield 5-alkoxyisoxazolidines using 1,4-cyclohexadienes as hydrogen donors.

ANTI-BACTERIAL COMPOSITIONS AND METHODS INCLUDING TARGETING VIRULENCE FACTORS OF STAPHYLOCOCCUS AUREUS

This disclosure relates to compositions and methods including for the inhibition, prevention, and/or treatment of microbial infections, including infections from such pathogens as Staphylococcus aureus.

Phosphonosulfonates are potent, selective inhibitors of dehydrosqualene synthase and staphyloxanthin biosynthesis in staphylococcus aureus

Staphylococcus aureus produces a golden carotenoid virulence factor called staphyloxanthin (STX), and we report here the inhibition of the enzyme, dehydrosqualene synthase (CrtM), responsible for the first committed step in STX biosynthesis. The most acti