39669-92-6 Usage
General Description
Tetradeca-1,3-diene is a chemical compound classified as an unsaturated hydrocarbon belonging to the category of alkenes. It is composed of two double bonds and fourteen carbon atoms, hence the name "tetradeca," meaning fourteen in Greek, and "diene," referring to the two double bonds. tetradeca-1,3-diene is characterized by a linear arrangement of carbon atoms. Like other alkenes, Tetradeca-1,3-diene could undergo reactions such as oxidation, halogenation, and polymerization. As an organic compound, it can be found in certain natural sources or produced through organic synthesis processes. Its properties, toxicity, and potential uses are subjects of scientific investigation and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 39669-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,6 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39669-92:
(7*3)+(6*9)+(5*6)+(4*6)+(3*9)+(2*9)+(1*2)=176
176 % 10 = 6
So 39669-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H26/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h3,5,7H,1,4,6,8-14H2,2H3
39669-92-6Relevant articles and documents
CONJUGATED DIENE PRODUCTION METHOD
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Paragraph 0039; 0040; 0041, (2018/09/30)
PROBLEM TO BE SOLVED: To provide a novel conjugated diene production method. SOLUTION: A method of producing a conjugated diene represented by the specified general formula (2) is characterized by reacting 1-acyloxy-1,3-alkadiene represented by the specified general formula (1) with a Grignard reagent represented by R6-Mg-X in the presence of an iron catalyst. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT
A simplified Wittig synthesis using a solid/liquid transfer process. IX. Selectivity of the condensation reaction of moderated ylides with aldehydes
Ben Attra,Le Bigot,El Gharbi,Delmas,Gaset
, p. 1421 - 1425 (2007/10/02)
Conjugated dienes are obtained selectively and with high yields using aldehydes of various structures. The synthesis is made in a two-phase medium, i.e. solid/liquid medium.
