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23144-52-7

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23144-52-7 Usage

Description

8-Chloro-1-octanol, a ω-chloro-1-alkanol, is a clear colorless liquid with significant potential in various scientific and industrial applications. Its unique chemical structure allows it to be utilized in a range of processes, from the synthesis of complex organic compounds to exhibiting antifungal properties.

Uses

Used in Chemical Synthesis:
8-Chloro-1-octanol is used as a key intermediate in the synthesis of various organic compounds for different applications. It plays a crucial role in the following processes:
1. Biosynthesis of bacteriochlorophyll c derivatives, where it is used for esterification.
2. Preparation of new macroporous triisobutylphosphine sulphide functionalized polymers, contributing to the development of advanced materials.
3. Synthesis of a series of new mesogenic azomethine diols, which are essential for creating novel liquid crystal materials.
4. Synthesis of bis(4-hydroxyoctoxyphenyl)sulfone (HOS), a compound with potential applications in various industries.
Used in Pharmaceutical and Biotechnology Industry:
8-Chloro-1-octanol is used as an active ingredient for its antifungal properties, particularly against the following fungi:
1. Aspergillus niger
2. Trichoderma viride
3. Myrothecium verrucaria
4. Candida albicans
5. Trichophyton mentagrophytes
6. Mucor mucedo
Its effectiveness in inhibiting the growth of these fungi makes it a valuable asset in the development of antifungal agents and treatments, particularly in the pharmaceutical and biotechnology sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 23144-52-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23144-52:
(7*2)+(6*3)+(5*1)+(4*4)+(3*4)+(2*5)+(1*2)=77
77 % 10 = 7
So 23144-52-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H17ClO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2

23144-52-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H28417)  8-Chloro-1-octanol, 98%   

  • 23144-52-7

  • 5ml

  • 359.0CNY

  • Detail
  • Alfa Aesar

  • (H28417)  8-Chloro-1-octanol, 98%   

  • 23144-52-7

  • 25ml

  • 1377.0CNY

  • Detail

23144-52-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-chlorooctan-1-ol

1.2 Other means of identification

Product number -
Other names 8-Chlor-octylalkohol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:23144-52-7 SDS

23144-52-7Relevant articles and documents

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

Magee,Mayo,Silk,Beattie

, p. 1368 - 1377 (2013/05/22)

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

Kasymzhanova, M.,Abdukakharov, V. S.,Kamaev, F. G.,Abduvakhabov, A. A.

, p. 708 - 713 (2007/10/02)

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

Kovalev, B. G.,Matveeva, E. D.,Stan, V. V.,Vovk, G. A.,Yudin, L. G.,Kost, A. N.

, p. 1728 - 1733 (2007/10/02)

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

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