16487-68-6 Usage
Uses
Used in Polymer and Resin Production:
2,3-Octadiene is used as a monomer in the production of polymers and resins, contributing to the creation of various materials with specific properties for different applications.
Used in Synthetic Rubber Industry:
In the synthetic rubber industry, 2,3-Octadiene is utilized as a monomer for the production of synthetic rubber, which is essential for manufacturing a wide range of rubber-based products.
Used as a Chemical Intermediate in Pharmaceutical Synthesis:
2,3-Octadiene serves as a chemical intermediate in the synthesis of pharmaceuticals, playing a crucial role in the development of various medications.
Used as a Chemical Intermediate in Agrochemical Synthesis:
Similarly, in the agrochemical industry, 2,3-Octadiene is employed as a chemical intermediate, aiding in the production of various agrochemicals that are vital for agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 16487-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16487-68:
(7*1)+(6*6)+(5*4)+(4*8)+(3*7)+(2*6)+(1*8)=136
136 % 10 = 6
So 16487-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-3-5-7-8-6-4-2/h3,7H,4,6,8H2,1-2H3
16487-68-6Relevant academic research and scientific papers
Barluenga, Jose,Fernandez, Jose R.,Yus, Miguel
, p. 203 - 204 (1985)
Unsaturated chlorohydrins (1) (readily obtained from crotonaldehyde) are converted, by methylation and in situ lithiation at room temperature, into alka-2,3-dienes (2).
REACTIONS OF 3-ALKYL- AND 3,3-DIALKYL-1-BROMOALLENES WITH ORGANOCUPRATES: EFFECTS OF THE NATURE OF THE CUPRATE REAGENT ON THE REGIO- AND STEREOSELECTIVITY
Caporusso, Anna Maria,Polizzi, Carmela,Lardicci, Luciano
, p. 6073 - 6076 (2007/10/02)
Organocuprates induce 1,3- and direct substitution in 3-alkyl- and 3,3-dialkyl-1-bromo-1,2-dienes leading respectively to either terminal acetylenes or allenic hydrocarbons.The nature of the cuprate exerts a prominent role in determining both the regio- and the stereochemistry of these reactions.
