Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate

Base Information

Chemical Name:Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate
CAS No.:75862-78-1
Molecular Formula:C11H14O2
Molecular Weight:178.231
Hs Code.:
DSSTox Substance ID:DTXSID30506348
Nikkaji Number:J2.155.170H

Synonyms:ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate;75862-78-1;DTXSID30506348

Suppliers and Price of Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate

Supply Marketing:

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

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Chemical Property of Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:178.099379685
Heavy Atom Count:13
Complexity:272

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1C=CC=CC=C1C

Technology Process of Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate

There total 1 articles about Ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate 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:

: 623-73-4
diazoacetic acid ethyl ester

: 75-09-2
dichloromethane

: 108-88-3,15644-74-3,16713-13-6
toluene

: 6628-21-3
ethyl 2,3-dichloropropionate

: 75862-78-1
ethyl 2-methylcyclohepta-2,4,6-triene-1-carboxylate

: 75862-72-5
ethyl 4-methylcyclohepta-2,4,6-triene-1-carboxylate

: 75862-75-8
ethyl 3-methylcyclohepta-2,4,6-triene-1-carboxylate

Guidance literature:: [HB(3,5-(CF₃)2Pz)3]^(1-) derivative; In dichloromethane; at 20 ℃; Further byproducts given;
DOI:10.1016/j.tetlet.2005.02.052