2,3-Dimethyl-1,3-pentadiene

Base Information

Chemical Name:2,3-Dimethyl-1,3-pentadiene
CAS No.:1625-49-6
Molecular Formula:C7H12
Molecular Weight:96.1723
Hs Code.:
Nikkaji Number:J797.963K,J2.655.844A

Synonyms:2,3-Dimethyl-1,3-pentadiene;(E)-1,3-Pentadiene, 2,3-dimethyl-;1625-49-6;1,3-Pentadiene, 2,3-dimethyl-;PCCCQOGUVCNYOI-FNORWQNLSA-N;(3E)-2,3-Dimethyl-1,3-pentadiene;AKOS006275132;(3E)-2,3-dimethyl-penta-1,3-diene;(3E)-2,3-Dimethyl-1,3-pentadiene #;(E)-CH3CH=C(CH3)C(CH3)=CH2

Suppliers and Price of 2,3-Dimethyl-1,3-pentadiene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2,3-Dimethyl-1,3-pentadiene

Chemical Property:

Vapor Pressure:41.9mmHg at 25°C
Boiling Point:100.6°C at 760 mmHg
Density:0.726g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:96.093900383
Heavy Atom Count:7
Complexity:96.6

Purity/Quality:

Safty Information:

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MSDS Files:

Useful:

Canonical SMILES:CC=C(C)C(=C)C
Isomeric SMILES:C/C=C(\C)/C(=C)C
General Description (3E)-2,3-Dimethylpenta-1,3-diene is a conjugated diene that has been studied in the context of Diels-Alder reactions, particularly with juglone, to investigate regioselectivity and the role of secondary orbital interactions (SOI). The uncatalyzed and catalyzed reactions of this diene demonstrate regioselectivity consistent with frontier molecular orbital (FMO) theory when considering SOI, though steric effects from bulky catalysts can alter product distributions. Computational analyses support a zwitterionic mechanism in catalyzed reactions, with SOI contributing to transition-state stabilization and pathway control.

Technology Process of 2,3-Dimethyl-1,3-pentadiene

There total 8 articles about 2,3-Dimethyl-1,3-pentadiene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%