Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate

Base Information

Chemical Name:Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate
CAS No.:89709-98-8
Molecular Formula:C12H20O6
Molecular Weight:260.287
Hs Code.:
DSSTox Substance ID:DTXSID40534652

Synonyms:89709-98-8;Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate;DTXSID40534652

Suppliers and Price of Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:9
Exact Mass:260.12598835
Heavy Atom Count:18
Complexity:292

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(C1CC1(C(=O)OC)C(=O)OC)OCC

Technology Process of Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate

There total 1 articles about Dimethyl 2-(diethoxymethyl)cyclopropane-1,1-dicarboxylate 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:

: 3054-95-3
acrylaldehyde diethyl acetal

: 6773-29-1
dimethyl diazomalonate

: 817-95-8
ethyl 2-ethoxyethanoate

: 89709-96-6
methyl 2-carbomethoxy-2,5-diethoxy-(E)-4-pentenoate

: 89709-97-7
methyl 2-carbomethoxy-2,3-diethoxy-4-pentenoate

: 89709-98-8
dimethyl 2-(diethoxymethyl)-1,1-cyclopropanedicarboxylate

Guidance literature:: dirhodium tetraacetate; at 40 ℃; for 8h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00185a014