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Cyclotetradecene, (E)is a chemical compound with the molecular formula C14H26. It is a colorless liquid and a type of alkene, which means it contains a carbon-carbon double bond in a specific geometric orientation (E configuration). Cyclotetradecene, (E)is known for its versatility as a building block in organic chemistry and its ability to act as a precursor in the synthesis of other chemicals.

114336-03-7

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114336-03-7 Usage

Uses

Used in Chemical Synthesis:
Cyclotetradecene, (E)is used as a precursor in the synthesis of other chemicals for various applications. Its unique structure and properties make it a valuable component in the production of a wide range of chemical compounds.
Used in Industrial and Consumer Products:
Cyclotetradecene, (E)is used in the production of various industrial and consumer products, such as adhesives, sealants, lubricants, and plastics. Its versatility and chemical properties contribute to the performance and quality of these products.
Used in Environmental Research:
Cyclotetradecene, (E)has been identified as a potential environmental pollutant, and its presence may have harmful effects on aquatic organisms. As a result, it is used in environmental research to study its impact on ecosystems and develop methods to mitigate its effects.
Used in Adhesives Industry:
Cyclotetradecene, (E)is used as a component in the formulation of adhesives for various applications. Its chemical properties contribute to the adhesive's performance, such as bonding strength and durability.
Used in Sealants Industry:
Cyclotetradecene, (E)is used in the production of sealants, which are essential for sealing joints and preventing the passage of air, water, or other substances. Its properties enhance the sealant's effectiveness and longevity.
Used in Lubricants Industry:
Cyclotetradecene, (E)is used as a component in lubricants to reduce friction and wear between moving parts in various mechanical systems. Its properties improve the lubricant's performance and extend the life of the machinery.
Used in Plastics Industry:
Cyclotetradecene, (E)is used in the manufacturing of plastics, contributing to their properties such as flexibility, strength, and durability. Its presence in plastic formulations helps to create a wide range of plastic products for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 114336-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,3 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 114336-03:
(8*1)+(7*1)+(6*4)+(5*3)+(4*3)+(3*6)+(2*0)+(1*3)=87
87 % 10 = 7
So 114336-03-7 is a valid CAS Registry Number.

114336-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclotetradecene

1.2 Other means of identification

Product number -
Other names -

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:114336-03-7 SDS

114336-03-7Downstream Products

114336-03-7Relevant academic research and scientific papers

A Simple Synthesis of Macrocyclic Hydrocarbons by Metathesis of Cycloolefins

Warwel, Siegfried,Kaetker, Hans

, p. 935 - 937 (1987)

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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