32763-70-5 Usage
Description
Trans-5-Methyl-1,3-hexadiene, also known as 5-Methyl-1,3-hexadiene, is an organic compound with the molecular formula C7H12. It belongs to the class of alkenes and contains a double bond between the second and third carbon atoms. This colorless liquid has a strong, pungent odor and is used as a chemical intermediate in various industries.
Uses
Used in Chemical Industry:
Trans-5-Methyl-1,3-hexadiene is used as a chemical intermediate for the production of various organic compounds, such as plastics, resins, and solvents. Its unique structure and properties make it a valuable component in the synthesis of these materials.
Used in Laboratory Research:
trans-5-Methyl-1,3-hexadiene is also utilized in laboratory research for studying chemical reactions and processes involving alkenes. Its reactivity and stability make it a useful tool for understanding the behavior of similar compounds.
Used in Fragrance and Flavor Industry:
Trans-5-Methyl-1,3-hexadiene is used as a component in the production of fragrances and flavors, adding unique scents and tastes to various products. Its strong, pungent odor contributes to the overall sensory experience of these products.
Safety Precautions:
It is important to handle trans-5-Methyl-1,3-hexadiene with caution, as it may be flammable and harmful if inhaled, ingested, or in contact with the skin. Proper safety measures should be taken to minimize risks during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 32763-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,7,6 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32763-70:
(7*3)+(6*2)+(5*7)+(4*6)+(3*3)+(2*7)+(1*0)=115
115 % 10 = 5
So 32763-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H12/c1-4-5-6-7(2)3/h4-7H,1H2,2-3H3/b6-5+
32763-70-5Relevant articles and documents
Catalytic hydromagnesation of di- and polymethyl-substituted 1,3-butadienes
Viktorov,Zubritskii
, p. 1755 - 1765 (2007/10/03)
Hydromagnesation of di- and polymethyl-substituted 1,3-butadienes with alkylmagnesium halides in the presence of Ni(PPh3)2Cl2 and NiPy4Cl2 was studied.
Une synthese hautement stereoselective de dienes conjugues (E)
Bloch, R.,Abecassis, J.,Hassan, D.
, p. 2019 - 2024 (2007/10/02)
A general method for the preparation of (E) terminal conjugated dienes was developed by the flash thermolysis of 2-substituted 2,5-dihydrothiophene-1,1-dioxides generated by a retro Diels-Alder reaction.This process allows the obtention of conjugated dienes, bearing or not a functionality (alcohols, esters), with an excellent stereoisomeric purity (in general higher than 98percent).An application to the synthesis of (E)-9,11-dodecadien-1-yl acetate, the major component of the sex pheromone of Diparopsis castanea, shows the generality and the efficacy of this method.
