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

Description

4-(4-N-BUTYLPHENYL)BENZALDEHYDE is a benzaldehyde derivative that is an aromatic compound with a benzene ring substituted with a butyl group and a benzaldehyde functional group. It has potential applications in the field of organic synthesis and chemical research due to its unique structure and reactivity.
Used in Organic Synthesis:
4-(4-N-BUTYLPHENYL)BENZALDEHYDE is used as a building block for the synthesis of more complex organic compounds and pharmaceutical products. Its unique structure and reactivity make it a valuable component in the creation of new molecules.
Used in Chemical Research:
4-(4-N-BUTYLPHENYL)BENZALDEHYDE is used as a research compound to study its properties and potential applications in various chemical reactions and processes. Its unique structure allows for exploration of its reactivity and behavior in different chemical environments.
Used in Pharmaceutical Industry:
4-(4-N-BUTYLPHENYL)BENZALDEHYDE is used as an intermediate in the synthesis of pharmaceutical products. Its unique structure and reactivity make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Fragrance Industry:
4-(4-N-BUTYLPHENYL)BENZALDEHYDE is used as a fragrance ingredient in the creation of various scented products. Its aromatic nature and unique scent profile make it a valuable component in the formulation of perfumes, colognes, and other fragranced products.

Upstream product

• 52709-83-8 4'-n-butyl-4-cyanobiphenyl 
• 92-52-4 biphenyl 
• 37909-95-8 4-butylbiphenyl 
• 13211-01-3 1-([1,1'-biphenyl]-4-yl)butan-1-one 
• 93972-13-5 4'-Butyl-biphenyl-4-carbaldehyde oxime 
• 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, 

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.

SYSTEM FOR CONTROLLING THE REACTIVITY OF BORONIC ACIDS

A protected organoboronic acid includes a boron having an sp3 hybridization, a conformationally rigid protecting group bonded to the boron, and an organic group bonded to the boron through a boron-carbon bond. A method of performing a chemical reaction includes contacting a protected organoboronic acid with a reagent, the protected organoboronic acid including a boron having an sp3 hybridization, a conformationally rigid protecting group bonded to the boron, and an organic group bonded to the boron through a boron-carbon bond. The organic group is chemically transformed, and the boron is not chemically transformed.