118578-88-4

Basic information

• Product Name: Benzenemethanol, 4-hexyl-
• CAS NO: 118578-88-4
• Molecular Formula: C13H20O
• Molecular Weight: 192.301
• Mol File: 118578-88-4.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 4-hexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 4-hexyl-(118578-88-4)
• EPA Substance Registry System: Benzenemethanol, 4-hexyl-(118578-88-4)

Safety Data

• Hazardous Substances Data: 118578-88-4(Hazardous Substances Data)

Usage

General Description

Benzenemethanol, 4-hexyl- is a chemical compound with the formula C14H22O. It is an aromatic alcohol with a six-carbon chain attached to the benzene ring. Benzenemethanol, 4-hexyl- is used in the production of perfumes and flavorings, as well as in the synthesis of other organic compounds. It is also used in the manufacturing of plasticizers, which are added to plastics to improve their flexibility and durability. Additionally, Benzenemethanol, 4-hexyl- has potential applications in the pharmaceutical industry, particularly in the development of drugs and medicines. However, its use raises concerns about its toxicological properties and potential environmental impact, as it may pose risks to human health and the environment if not properly managed.

Upstream product

• 79-37-8 oxalyl dichloride 
• 1077-16-3 hexylbenzene 
• 59016-93-2 p-hydroxymethylphenylboronic acid 
• 18282-51-4 4-iodo-benzyl alcohol 
• 50606-95-6 4-hexylbenzoyl chloride 
• 942-92-7 caprophenone 
• 142-61-0 Hexanoyl chloride 
• 71-43-2 benzene 
• 199786-54-4 (4-Hexyl-phenyl)-trimethyl-silane 
• 6999-03-7 1-bromo-4-(trimethylsilyl)benzene 
• 62150-34-9 1-n-hexyl-4-iodobenzene 
• 111-25-1 1-bromo-hexane 
• 89511-01-3 p-n-hexylbenzaldehyde diethylacetal 
• 49763-69-1 4-hexylbenzaldehyde 

Downstream Products

• 1439439-10-7 S-4-hexylbenzyl ethanethioate 
• 1439439-11-8 1,2-bis(4-hexylbenzyl)disulfane 
• 1439439-05-0 S-4-hexylbenzyl (4-hexylphenyl)methanethiosulfinate 
• 60982-73-2 4-hexylphenylacetonitrile 
• 82720-63-6 4-hexylphenylmethyl 6-cyano-2-naphthyl ether 
• 58999-67-0 1-chloromethyl-4-hexylbenzene 
• 60982-72-1 4-hexylbenzyl bromide 

Relevant articles and documents

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

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Copper-Catalyzed Boron-Selective C(sp2)-C(sp3) Oxidative Cross-Coupling of Arylboronic Acids and Alkyltrifluoroborates Involving a Single-Electron Transmetalation Process

A rapid and highly selective oxidative cross-coupling reaction between readily available and shelf-stable arylboronic acids and primary or secondary potassium alkyltrifluoroborates was devised and developed, which works under mild conditions using copper(II) acetate as the catalyst and silver oxide as the oxidant. Initial experimental results indicate that a single-electron transmetalation process is involved. This approach effectively bypasses the problems associated with the traditional cross-coupling reactions of alkylboronates and thus provides a complementary method in building C(sp2)-C(sp3) bonds.

Antioxidant generation and regeneration in lipid bilayers: The amazing case of lipophilic thiosulfinates and hydrophilic thiols

We demonstrate that the garlic-derived chemopreventive agent allicin and the related anamu-derived petivericin are poor radical-trapping antioxidants in lipid bilayers, but that the in situ reaction of a lipophilic analog and a hydrophilic thiol yields an extremely potent radical-trapping antioxidant that can be recycled in the presence of excess thiol.