4894-62-6 Usage
Description
(5E)-3-methylhepta-1,5-diene is a chemical compound with the molecular formula C8H14. It is a linear hydrocarbon that consists of a chain of seven carbon atoms with a methyl group attached to the third carbon and a double bond between the first and fifth carbon atoms. (5E)-3-methylhepta-1,5-diene belongs to the class of alkenes, which are organic compounds that contain carbon-carbon double bonds. Its specific structure and reactivity make it useful in organic synthesis and as a building block for more complex molecules.
Uses
Used in Chemical Synthesis:
(5E)-3-methylhepta-1,5-diene is used as a starting material for the production of various synthetic chemicals and polymers. Its unique structure and reactivity make it a valuable building block for creating more complex molecules.
Used in Polymer Production:
(5E)-3-methylhepta-1,5-diene is used as a monomer in the synthesis of polymers. Its carbon-carbon double bonds allow for polymerization reactions, resulting in the formation of polymers with specific properties and applications.
Used in Organic Synthesis:
(5E)-3-methylhepta-1,5-diene is used as a reactant in various organic synthesis processes. Its reactivity allows for the formation of new chemical bonds and the creation of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 4894-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4894-62:
(6*4)+(5*8)+(4*9)+(3*4)+(2*6)+(1*2)=126
126 % 10 = 6
So 4894-62-6 is a valid CAS Registry Number.
4894-62-6Relevant articles and documents
THERMISCHE STABILITAET VON BIS(ALK-2-ENYL)ZINK-VERBINDUNGEN
Lehmkuhl, Herbert,Doering, Ingo,Nehl, Hans
, p. 7 - 12 (2007/10/02)
The dialk-2-enylzinc compounds I-III react slowly at 20 to 50 deg C by addition of the Zn-C bond to the C=C bond of an alk-2-enyl group to give oligomers from which the alkenes XIII-XV are released on hydrolysis.For I-III homolytic cleavage of the Zn-Callyl bond, followed by coupling of the allyl radicals to give the alkadienes V-VII, IX and XI predominates above 50 deg C.IV decomposes mainly homolytically even at 20 deg C.
