68516-32-5 Usage
Description
(E)-tetradec-11-en-9-ynol, with the molecular formula C14H24O, is a synthetic alcohol characterized by a long hydrocarbon chain and a triple bond between carbon atoms. This chemical compound is known for its potential applications in various industries and its biological activities, such as antimicrobial and anti-inflammatory properties.
Uses
Used in Chemical Industry:
(E)-tetradec-11-en-9-ynol is used as a key component in the production of surfactants, lubricants, and plasticizers. Its unique structure allows it to enhance the performance and properties of these industrial products, making it a valuable asset in the chemical industry.
Used in Pharmaceutical Industry:
As a precursor in the synthesis of other organic compounds, (E)-tetradec-11-en-9-ynol plays a crucial role in the development of new pharmaceuticals. Its potential biological activities, including antimicrobial and anti-inflammatory properties, make it a promising candidate for further research and development in the pharmaceutical field.
Used in Research and Development:
Due to its versatile applications and potential for further exploration, (E)-tetradec-11-en-9-ynol is of interest to researchers in various fields. It serves as a foundation for the development of new materials, products, and compounds, contributing to the advancement of scientific knowledge and technological innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 68516-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,1 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68516-32:
(7*6)+(6*8)+(5*5)+(4*1)+(3*6)+(2*3)+(1*2)=145
145 % 10 = 5
So 68516-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h3-4,15H,2,7-14H2,1H3/b4-3+
68516-32-5Relevant articles and documents
PREPARATION OF 1,3-DIENES, ITS APPLICATION TO THE SYNTHESIS OF (Z,E)-9,11-TETRADECADIENYL ACETATE AND (E,E)-10,12-HEXADECADIENAL: SEX PHEROMONES OF COTTON PESTS
Yadav, J S,Deshpande, Prasad K,Reddy, E Rajarathnam
, p. 125 - 134 (2007/10/02)
E-2-Penten-4-yn-1-ol (3) has been utilized as a source for 1,3-diene systems by employing lithium amide induced alkylation, and curpous iodide catalysed Grignard coupling reaction as key steps.Its application for the synthesis of (Z,E)-9,11-tetradecadienyl acetate and (E,E)-10,12-hexadecadienal is described.
