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Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate

Base Information Edit
  • Chemical Name:Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate
  • CAS No.:7371-67-7
  • Molecular Formula:C8H12O4
  • Molecular Weight:172.181
  • Hs Code.:
  • Mol file:7371-67-7.mol
Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate

Synonyms:dimethyl trans-1,2-cyclobutanedicarboxylate;trans-1,2-cyclobutane dimethylcarboxylate;trans-1,2-cyclobutanedicarboxylic acid,dimethyl ester;(+/-)-trans-Cyclobutan-dicarbonsaeure-(1.2)-dimethylester;1,2-Cyclobutanedicarboxylic acid, dimethyl ester, trans-;dimethyl trans-cyclobutane-1,2-dicarboxylate;(+/-)-trans-cyclobutane-dicarboxylic acid-(1.2)-dimethyl ester;

Suppliers and Price of Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • A2B
  • 1,2-Cyclobutanedicarboxylicacid,dimethylester,trans- 97%
  • 250g
  • $ 13388.00
  • A2B
  • 1,2-Cyclobutanedicarboxylicacid,dimethylester,trans- 97%
  • 25g
  • $ 2575.00
  • A2B
  • 1,2-Cyclobutanedicarboxylicacid,dimethylester,trans- 97%
  • 5g
  • $ 773.00
Total 2 raw suppliers
Chemical Property of Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate Edit
Chemical Property:
  • Refractive Index:1.4450 (estimate) 
  • Boiling Point:225°C (estimate) 
  • PSA:52.60000 
  • Density:1.1276 
  • LogP:0.35860 
Purity/Quality:

95% *data from raw suppliers

1,2-Cyclobutanedicarboxylicacid,dimethylester,trans- 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate

There total 1 articles about Dimethyl trans-(+)-1,2-cyclobutanedicarboxylate 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:
Guidance literature:
With sulfuric acid; Yield given. Multistep reaction; 1.) CH3OH, reflux, 6 h, 2.) CH3OH, reflux, 12 h;
DOI:10.1021/ja00381a024
Guidance literature:
Multi-step reaction with 2 steps
1: 50 percent / LiALH4 / tetrahydrofuran
2: 69 percent
With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1021/ja00256a040
Refernces Edit
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