41446-53-1 Usage
Description
(3Z)-tridec-3-ene, with the molecular formula C13H26, is a long-chain unsaturated hydrocarbon. It is a 3Z isomer of tridecene, characterized by a double bond at the third carbon from the end of the carbon chain with a cis configuration. This chemical compound is known for its applications in various industries, including the production of organic chemicals, flavors, fragrances, and pharmaceuticals.
Uses
Used in Chemical Production:
(3Z)-tridec-3-ene is used as a precursor in the synthesis of various organic chemicals, such as polymers, solvents, and synthetic lubricants. Its unique structure and properties make it a valuable component in the development of these materials.
Used in Flavors and Fragrances:
(3Z)-tridec-3-ene is used as a key ingredient in the production of flavors and fragrances. Its natural presence in certain plant oils contributes to its use in creating distinct and appealing scents for various applications.
Used in Pharmaceutical Industry:
(3Z)-tridec-3-ene is used as a building block for the synthesis of various drug compounds in the pharmaceutical industry. Its versatility and chemical properties make it a promising candidate for the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 41446-53-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,4 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41446-53:
(7*4)+(6*1)+(5*4)+(4*4)+(3*6)+(2*5)+(1*3)=101
101 % 10 = 1
So 41446-53-1 is a valid CAS Registry Number.
41446-53-1Relevant articles and documents
Stabilization of long-chain intermediates in solution. octyl radicals and cations
Teodorovi?, Aleksandar V.,Badjuk, Dalibor M.,Stevanovi?, Nenad,Pavlovi?, Radoslav Z.
, p. 19 - 24 (2013/06/26)
The rearrangements of 1-octyl, 1-decyl and 1-tridecyl intermediates obtained from thermal lead(IV) acetate (LTA) decarboxylation of nonanoic, undecanoic and tetradecanoic acid were investigated experimentally through analysis and distribution of the products. The relationships between 1,5-, 1,6- and possibly existing 1,7-homolytic hydrogen transfer in 1-octyl-radical, as well as successive 1,2-hydride shift in corresponding cation have been computed via Monte-Carlo method. Taking into account that ratios of 1,5-/1,6-homolytic rearrangements in 1-octyl- and 1-tridecyl radical are approximately the same, the simulation shows very low involvement of 1,7-hydrogen rearrangement (1,5-/1,6-/1,7-hydrogen rearrangement = 85:31:1) in 1-octyl radical.
