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(3E,5Z)-4,5-Diethyl-3,5-octadiene is a colorless, liquid organic compound with the molecular formula C12H22. It belongs to the class of compounds known as alkenes and contains two double bonds in its structure. (3E,5Z)-4,5-Diethyl-3,5-octadiene is commonly used in the synthesis of other organic compounds and is known for its reactivity.

21293-02-7

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21293-02-7 Usage

Uses

Used in Fragrance and Flavor Industry:
(3E,5Z)-4,5-Diethyl-3,5-octadiene is used as a precursor in the production of fragrances and flavors. Its unique chemical structure allows it to be transformed into a variety of different scent and taste compounds, making it a valuable component in the creation of various consumer products.
Used in Fine Chemicals Industry:
(3E,5Z)-4,5-Diethyl-3,5-octadiene is also utilized in the synthesis of other fine chemicals. Its versatility and reactivity make it an essential building block for the development of specialty chemicals used in various industries.
Used in Organic Synthesis:
(3E,5Z)-4,5-Diethyl-3,5-octadiene serves as a precursor in the synthesis of a variety of different organic compounds. Its double bonds make it highly reactive, allowing it to be easily incorporated into more complex molecular structures, which is crucial for the development of new materials and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 21293-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,9 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21293-02:
(7*2)+(6*1)+(5*2)+(4*9)+(3*3)+(2*0)+(1*2)=77
77 % 10 = 7
So 21293-02-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H22/c1-5-9-11(7-3)12(8-4)10-6-2/h9-10H,5-8H2,1-4H3/b11-9-,12-10+

21293-02-7Downstream Products

21293-02-7Relevant academic research and scientific papers

Hydroboration. 69. Hydroboration Characteristics of Lithium Borohydride/Ethyl Acetate in Ethyl Ether. A New System for Controlled Hydroboration of Alkenes and Alkynes

Brown, Herbert C.,Somayaji, Vishwanatha,Narasimhan, S.

, p. 4822 - 4827 (2007/10/02)

Alkenes and alkynes, which are normally inert to lithium borohydride, are readily hydroborated by this reagent in ethyl ether in the presence of carboxylic esters at 25 deg C.Alkenes form dialkylborinates while alkynes give rise either to vinylboranates or divinylborinates, depending upon the structure and reactivity of the alkyne and the stoichiometry of the reagent.This valuable intermediates are readily transformed into other organic derivatives, thus making this controlled hydroboration procedure a practical, valuable procedure in organic synthesis.

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