23144-52-7

Basic information

• Product Name: 8-Chloro-1-octanol
• Synonyms: 8-chloro-1-octano;8-CHLOROOCTANOL;8-CHLOROOCTAN-1-OL;8-CHLORO-1-OCTANOL;8-CHLORO-11-OXYEN-10,11-2H-5-H-DIBENZO-[1,4]DIAZEPINE 8-CHLORO-1-OCTANOL;8-Chlor-octan-1-ol;8-CHLORO-1-OCTANOL 98+%;1-Chlorooctan-8-ol
• CAS NO: 23144-52-7
• Molecular Formula: C₈H₁₇ClO
• Molecular Weight: 164.67
• EINECS: 245-451-6
• Product Categories: Linear hydrocarbon series;Aliphatics;Alcohols;C7 to C8;Oxygen Compounds;OLED materials,pharm chemical,electronic
• Mol File: 23144-52-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 129-130 °C11 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: Clear colorless/Liquid
• Density: 0.976 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0105mmHg at 25°C
• Refractive Index: n20/D 1.458(lit.)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 15.19±0.10(Predicted)
• CAS DataBase Reference: 8-Chloro-1-octanol(CAS DataBase Reference)
• NIST Chemistry Reference: 8-Chloro-1-octanol(23144-52-7)
• EPA Substance Registry System: 8-Chloro-1-octanol(23144-52-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-36/38
• Safety Statements: 37/39-26-24/25
• WGK Germany: 3
• TSCA: Yes
• Hazardous Substances Data: 23144-52-7(Hazardous Substances Data)

Usage

Chemical Properties

clear colorless liquid

Uses

Different sources of media describe the Uses of 23144-52-7 differently. You can refer to the following data:
1. 8-Chloro-1-octanol may be employed for the following studies:Biosynthesis of bacteriochlorophyll c derivatives, via esterification. Preparation of new macroporous triisobutylphosphine sulphide functionalized polymers.Synthesis of series of new mesogenic azomethine diols.Synthesis of bis(4-hydroxyoctoxyphenyl)sulfone (HOS).
2. Antifungal activity against Aspergillus niger, Trichoderma viride, Myrothecium verrucaria, Candida albicans, Trichophyton mentagrophytes, Mucor mucedo

General Description

8-Chloro-1-octanol is a ω-chloro-1-alkanol.

InChI:InChI=1/C8H17ClO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2

Upstream product

• 64-17-5 ethanol 
• 1427195-71-8 C₁₁H₂₀BrClO₂ 
• 1732-09-8 dimethyl subarate 
• 2050-23-9 diethyl suberate 
• 24088-97-9 8-chloro-oct-1-yne 
• 871-90-9 8-chloro-oct-1-ene 
• 629-41-4 1,8-Octanediol 

Downstream Products

• 5412-93-1 8-dibutylamino-octan-1-ol 
• 21524-76-5 4-amino-2-hydroxy-benzoic acid 8-morpholin-4-yl-octyl ester 
• 28598-82-5 1-bromo-8-chloro-octane 
• 1282454-61-8 C₃₀H₄₆O₈ 
• 1282453-71-7 C₆₄H₇₆O₈ 
• 1282453-78-4 C₆₆H₈₀O₈ 
• 1282453-81-9 C₇₄H₉₆O₈ 
• 155373-46-9 5-{[(8-Hydroxy-octyl)-phenyl-amino]-methylene}-2,2-dimethyl-[1,3]dioxane-4,6-dione 
• 19754-59-7 tetrahydro-2-(9-tetradecynyloxy)pyran 
• 945020-75-7 2-(4-hydroxyphenyl)-5-(8-chlorooctyloxy)pyrimidine 

Relevant articles and documents

Synthesis of (3E)-dodecen-12-olide, a potential pheromone component of the emerald ash borer

Emerald ash borer (EAB), Agrilus planipennis Fairmaire, is an invasive insect that has killed millions of ash trees in the USA and Canada. A concise synthesis of a potential EAB pheromone component, (3E)-dodecen-12-olide, using highly stereoselective Julia-Kocienski olefination as the key step, is reported. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.

SYNTHESIS OF THE SEX PHEROMONE OF THE GRAIN MOTH Ephestia Elutella

A most convenient synthesis of tetradeca-9Z,12E-dien-1-ol and its acetate - components of the sex pheromone of the grain moth - has been carried out on the basis of a scheme for obtaining a cis-1,trans-4-dienic system.

SYNTHESIS OF HIGHER ACETYLENIC ALCOHOLS

The alkylation of 1-alkynes in various solvents was investigated, and the optimum conditions for the production of acetylenic alcohols were obtained.