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Cyclooctene, 5-chloro-, also known as 5-chlorocyclooctene, is a chemical compound with the molecular formula C8H13Cl. It is a halogenated cycloalkene, featuring a cyclooctene ring with a chlorine atom attached at the 5th carbon position. Cyclooctene, 5-chloro- is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as a precursor for the production of other organic compounds. Cyclooctene, 5-chloro-, is a colorless to pale yellow liquid with a pungent odor and is insoluble in water but soluble in organic solvents. It is sensitive to light, heat, and moisture, and should be stored in a cool, dry place away from direct sunlight. Due to its potential reactivity and toxicity, appropriate safety measures should be taken when handling Cyclooctene, 5-chloro-.

1855-55-6

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1855-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1855-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1855-55:
(6*1)+(5*8)+(4*5)+(3*5)+(2*5)+(1*5)=96
96 % 10 = 6
So 1855-55-6 is a valid CAS Registry Number.

1855-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chlorocyclooctene

1.2 Other means of identification

Product number -
Other names 5-chloro-1-cyclooctene

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:1855-55-6 SDS

1855-55-6Downstream Products

1855-55-6Relevant academic research and scientific papers

Telomerization of Z,Z-cyclooctadiene with halomethanes catalyzed by chromium, copper, and molybdenum compounds in the presence of water

Khusnutdinov,Shchadneva,Oshnyakova,Dzhemilev

experimental part, p. 435 - 441 (2012/04/23)

The telomerization of 1Z,5Z-cyclooctadiene with halogenated methanes (CCl4, CBrCl3, CHCl3, CH2Cl 2) mediated by chromium, copper, and molybdenum complexes has been investigated. It has been shown that the use of water as a nucleophilic additive promotes the formation of 1,4- and 1,5-epoxycyclooctanes and anti-8-(trichloromethyl)bicyclo[3.2.1]octan-exo-2-ol. Pleiades Publishing, Ltd., 2011.

Novel transition-metal-free heterogeneous epoxidation catalysts discovered by means of high-throughput experimentation

Pescarmona, Paolo P.,Janssen, Kris P. F.,Jacobs, Pierre A.

, p. 6562 - 6572 (2008/03/15)

Various transition-metal-free oxides have been studied as catalysts for the epoxidation of cyclooctene with hydrogen peroxide by means of high-throughput experimentation. Different boron, aluminium, and gallium oxides were prepared according to various synthesis methods. A number of pure aluminium and gallium oxides showed very good catalytic performances, while the results obtained with boron oxides or mixed oxides were less positive. The best results were obtained with a gallium oxide catalyst, which gave an epoxide yield of 71 % and a selectivity of 99% after reaction for 4 h at 80°C. Gallium oxides had not been reported previously as active epoxidation catalysts. The use of high-throughput experimentation proved useful both for discovering new active catalysts and for identifying a number of relationships between the synthesis conditions and the catalytic properties of the transition-metal-free oxides.

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