rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate

Base Information

Chemical Name:rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate
CAS No.:424820-24-6
Molecular Formula:C₁₃H₁₄O₄
Molecular Weight:234.252
Hs Code.:
DSSTox Substance ID:DTXSID701173396
Nikkaji Number:J880.267J

Synonyms:DTXSID701173396;424820-24-6;rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate

Suppliers and Price of rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:234.08920892
Heavy Atom Count:17
Complexity:285

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C1C(C1C(=O)OC)C2=CC=CC=C2
Isomeric SMILES:COC(=O)[C@@H]1[C@@H](C1C2=CC=CC=C2)C(=O)OC

Technology Process of rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate

There total 1 articles about rel-1,2-Dimethyl (1R,2S)-3-phenyl-1,2-cyclopropanedicarboxylate 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:

: 98-87-3
benzylidene dichloride

: 624-48-6
dimethyl cis-but-2-ene-1,4-dioate

: 424820-24-6
3-Phenyl-cyclopropan-1,2-dicarbonsaeure-methylester

: 20098-66-2
(+/-)-3-phenyl-cyclopropane-1r,2t-dicarboxylic acid dimethyl ester

Guidance literature:: With tetrabutylammomium bromide; tetra-(n-butyl)ammonium iodide; In N,N-dimethyl-formamide; at 20 ℃; Product distribution;
DOI:10.1016/S0040-4020(01)01133-4