1-Ethenyl-2-methylcyclohex-1-ene

Base Information

Chemical Name:1-Ethenyl-2-methylcyclohex-1-ene
CAS No.:23155-97-7
Molecular Formula:C₉H₁₄
Molecular Weight:122.21
Hs Code.:
DSSTox Substance ID:DTXSID00539668
Nikkaji Number:J2.111.480D
Wikidata:Q82415459
Mol file:23155-97-7.mol

Synonyms:23155-97-7;1-Ethenyl-2-methylcyclohex-1-ene;DTXSID00539668

Suppliers and Price of 1-Ethenyl-2-methylcyclohex-1-ene

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 0 raw suppliers

Chemical Property of 1-Ethenyl-2-methylcyclohex-1-ene

Chemical Property:

Boiling Point:156-157 °C
PSA：0.00000
Density:0.894±0.06 g/cm3(Predicted)
LogP:3.06290
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:122.109550447
Heavy Atom Count:9
Complexity:140

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(CCCC1)C=C

Technology Process of 1-Ethenyl-2-methylcyclohex-1-ene

There total 4 articles about 1-Ethenyl-2-methylcyclohex-1-ene 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:

: 1-(2-methylcyclohex-1-en-1-yl)ethan-1-ol

: 23155-97-7
1-Vinyl-2-methylcyclohexene

Guidance literature:: With pyridine; dmap; In diethyl ether; at 0 ℃; for 1h;
DOI:10.1055/s-2007-973881

Reference yield:

: 4-methyl-3-vinyl-cyclohex-3-enol

: 23155-97-7
1-Vinyl-2-methylcyclohexene

Guidance literature:: With pyridine; methanesulfonyl chloride; Erwaermen des Reaktionsprodukts mit Lithiumalanat in Aether;
DOI:10.1021/ja01109a046