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Cyclotetradecene, specifically (Z)-Cyclotetradecene, is a cyclic alkene with the molecular formula C14H26. It features a 14-carbon ring structure with a double bond between two adjacent carbon atoms, giving it the Z configuration, which refers to the arrangement of substituents around the double bond. This organic compound is known for its unique chemical properties and potential applications in various industries, such as pharmaceuticals and materials science. Due to its cyclic nature and double bond, (Z)-Cyclotetradecene exhibits different reactivity and physical properties compared to linear alkenes, making it an interesting subject for chemical research and development.

2484-64-2

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2484-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2484-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,8 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2484-64:
(6*2)+(5*4)+(4*8)+(3*4)+(2*6)+(1*4)=92
92 % 10 = 2
So 2484-64-2 is a valid CAS Registry Number.

2484-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-cyclotetradecene

1.2 Other means of identification

Product number -
Other names cis-Cyclotetradecen

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:2484-64-2 SDS

2484-64-2Relevant academic research and scientific papers

A Simple Synthesis of Macrocyclic Hydrocarbons by Metathesis of Cycloolefins

Warwel, Siegfried,Kaetker, Hans

, p. 935 - 937 (2007/10/02)

Metathesis of cycloolefins normally leads to unsaturated polymers.Using rheniumheptoxide on alumina, activated by tintetramethyl and working in dilution via soxhlet-similiar circulation system the metathesis reaction was directed to macrocyclic dienes, which are the dimers of the initial cyclolefins.Starting with C7-, C9- and C10-cycloolefins symmetric macrocyclic C14-, C18- and C20-dienes are obtained in yields of 58-74percent.The metathetic dimerization of cyclooctene leads to 1,9-cyclohexadecadiene in a yield of 30percent.By hydrogenation at room temperature and normalhydrogen-pressure all cyclodienes were converted quantitatively to cycloalkenes (catalyst: potassium on alumina) or to cycloalkanes (catalyst: palladium on carbon).

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