5665-75-8

Basic information

• Product Name: 1-Hexanol, 2-(phenylmethylene)-
• CAS NO: 5665-75-8
• Molecular Formula: C13H18O
• Molecular Weight: 190.285
• Mol File: 5665-75-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-Hexanol, 2-(phenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hexanol, 2-(phenylmethylene)-(5665-75-8)
• EPA Substance Registry System: 1-Hexanol, 2-(phenylmethylene)-(5665-75-8)

Safety Data

• Hazardous Substances Data: 5665-75-8(Hazardous Substances Data)

Usage

General Description

1-Hexanol, 2-(phenylmethylene)-, also known as benzyl hexyl alcohol, is an organic compound with the chemical formula C13H18O. It is a colorless liquid with a floral odor, commonly used as a fragrance ingredient in perfumes and cosmetics. It is also used as a solvent in various industries, including pharmaceuticals and food processing. Additionally, 1-Hexanol, 2-(phenylmethylene)- has been studied for its potential antimicrobial properties and is considered safe for use in consumer products when used in accordance with regulations.

Upstream product

• 7492-44-6 2-n-butyl-3-phenyl-2-propenal 
• 4426-47-5 butylboronic acid 
• 66820-54-0 β-bromocinnamyl alcohol 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 109-72-8 n-butyllithium 

Relevant articles and documents

Nickel-Catalyzed Arylboration of Alkenylarenes: Synthesis of Boron-Substituted Quaternary Carbons and Regiodivergent Reactions

A method for the construction of boron-substituted quaternary carbons or diarylquaternary carbons by arylboration of highly substituted alkenylarenes is presented. A wide range of alkenes and arylbromides can participate in this reaction thus allowing for a diverse assortment of products to be prepared. In addition, a solvent dependent regiodivergent arylboration of 1,2-disubstituted alkenylarenes is presented, thus greatly increasing the scope of products that can be accessed.

Application of LB-Phos·HBF4 in the Suzuki coupling reaction of 2-bromoalken-3-ols with alkylboronic acids

LB-Phos·HBF4 was used in the Suzuki coupling reaction of 2-bromoalken-3-ols with alkylboronic acids to give the coupling products in moderate to good yields. Substituents such as benzyl, phenyl, allyl, and alkyl are tolerated at the 1-and 3-pos

Allyl alcohols and organocerium reagents, II. - Mechanism and extensibility of the reaction

Alkylcerium reagents add to the multiple bonds of allyl and propargyl alcohols in good yields and under mild conditions. The double bond can be reduced with lithium aluminum hydride in the presence of cerium trichloride. The regiochemistry of the attack depends on electronic factors.