692-96-6 Usage
Uses
Used in Chemical Production:
(E)-2-methylhept-3-ene is used as a precursor for the production of plasticizers, synthetic rubber, and other industrial chemicals. Its carbon-carbon double bond allows for various chemical reactions, making it a versatile building block in the chemical industry.
Used in Flavor and Fragrance Industry:
(E)-2-methylhept-3-ene is used as a component in the production of flavor and fragrance compounds. Its unique chemical structure contributes to the development of distinct scents and tastes, enhancing the sensory experience of various products.
Used in Organic Synthesis:
(E)-2-methylhept-3-ene is utilized as a reagent in various chemical reactions, playing a crucial role in organic synthesis. Its ability to participate in addition, polymerization, and other reactions makes it a valuable tool for creating new compounds and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 692-96-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 692-96:
(5*6)+(4*9)+(3*2)+(2*9)+(1*6)=96
96 % 10 = 6
So 692-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-4-5-6-7-8(2)3/h6-8H,4-5H2,1-3H3/b7-6-
692-96-6Relevant academic research and scientific papers
High yield of liquid range olefins obtained by converting i-propanol over zeolite H-ZSM-5
Mentzel, Uffe V.,Shunmugavel, Saravanamurugan,Hruby, Sarah L.,Christensen, Claus H.,Holm, Martin S.
experimental part, p. 17009 - 17013 (2010/03/23)
Methanol, ethanol, and i-propanol were converted under methanol-to-gasoline (MTH)-like conditions (400°C, 1-20 bar) over zeolite H-ZSM-5. For methanol and ethanol, the catalyst lifetimes and conversion capacities are comparable, but when i-propanol is use
HOMOALLYLIC SUBSTITUTION REACTIONS OF LITHIUM DIALKYL CUPRATES WITH CYCLOPROPYLCARBINYL HALIDES: MECHANISTIC CONSIDERATIONS
Hrubiec, Robert T.,Smith, Michael B.
, p. 1457 - 1468 (2007/10/02)
Highly reactive lithium dialkyl cuprates and 1-bromo-1-cyclopropylalkanes, 4, react to give good yields of the homoallylic substitution product, 6.Less reactive organocuprates react with 4 to give mixtures of 6 and the direct substitution product 7.These results are consistent with a copper(I) radical intermediate which undergoes facile rearrangement prior to reductive coupling.
