81500-71-2 Usage
Description
(12Z)-heptadeca-1,12-diene is a long-chain diene chemical compound that belongs to the class of organic compounds known as alkenes. It features a 12-carbon chain with a carbon-carbon double bond at the 12th position from the terminal carbon, giving it the (12Z) configuration. (12Z)-heptadeca-1,12-diene is commonly used as a building block in the synthesis of various organic compounds and can be found in natural sources such as essential oils and plant extracts. Its chemical structure and properties make it suitable for applications in the production of polymers, lubricants, and other industrial products.
Uses
Used in Chemical Synthesis:
(12Z)-heptadeca-1,12-diene is used as a building block in the synthesis of various organic compounds due to its unique chemical structure and properties.
Used in Polymer Production:
(12Z)-heptadeca-1,12-diene is used as a monomer in the production of polymers, contributing to the development of new materials with specific properties.
Used in Lubricant Industry:
(12Z)-heptadeca-1,12-diene is used as a component in the formulation of lubricants, enhancing their performance and reducing friction in various applications.
Used in Essential Oils and Plant Extracts:
(12Z)-heptadeca-1,12-diene is found in natural sources such as essential oils and plant extracts, where it contributes to the unique characteristics and potential applications of these natural products.
Check Digit Verification of cas no
The CAS Registry Mumber 81500-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,0 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81500-71:
(7*8)+(6*1)+(5*5)+(4*0)+(3*0)+(2*7)+(1*1)=102
102 % 10 = 2
So 81500-71-2 is a valid CAS Registry Number.
81500-71-2Relevant articles and documents
1,(ω-1)-Dienes: solvent controlled unilateral or bilateral metallation
Moret, Etienne,Desponds, Olivier,Schlosser, Manfred
, p. 83 - 91 (2007/10/02)
In hexane, i.e. under heterogeneous conditions, 1,(ω-1)-dienes readily undergo double deprotonation to give bis(allylmetal) intermediates.In tetrahydrofuran at -75 or -50 deg C, however, only monometallation occurs with dienes having chains of up to 12 carbon atoms.The practical potential of such selective monosubstitution reactions is demonstrated by two novel pheromone syntheses.
