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tetramethyl-1,2,3,4-cyclobutanetetracarboxylate

Base Information
  • Chemical Name:tetramethyl-1,2,3,4-cyclobutanetetracarboxylate
  • CAS No.:14495-41-1
  • Molecular Formula:C12H16 O8
  • Molecular Weight:288.254
  • Hs Code.:2917209090
  • Mol file:14495-41-1.mol
tetramethyl-1,2,3,4-cyclobutanetetracarboxylate

Synonyms:1,2,3,4-Cyclobutanetetracarboxylicacid, tetramethyl ester (6CI,7CI,8CI,9CI); Tetramethyl cyclobutane-1,2,3,4-tetracarboxylate

Suppliers and Price of tetramethyl-1,2,3,4-cyclobutanetetracarboxylate
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
  • Packaging
  • price
  • TRC
  • 1,2,3,4-CyclobutanetetracarboxylicAcid1,2,3,4-TetramethylEster
  • 500mg
  • $ 245.00
  • TCI Chemical
  • Tetramethyl 1,2,3,4-Cyclobutanetetracarboxylate >98.0%(GC)
  • 5g
  • $ 221.00
  • Sigma-Aldrich
  • CYCLOBUTANE-1,2,3,4-TETRACARBOXYLIC ACID TETRAMETHYL ESTER Aldrich
  • 100mg
  • $ 139.00
  • American Custom Chemicals Corporation
  • CYCLOBUTANE-1,2,3,4-TETRACARBOXYLIC ACID TETRAMETHYL ESTER 95.00%
  • 1G
  • $ 626.43
Total 24 raw suppliers
Chemical Property of tetramethyl-1,2,3,4-cyclobutanetetracarboxylate
Chemical Property:
  • Melting Point:145.0 to 149.0 °C 
  • PSA:105.20000 
  • LogP:-0.84320 
Purity/Quality:

98%,99%, *data from raw suppliers

1,2,3,4-CyclobutanetetracarboxylicAcid1,2,3,4-TetramethylEster *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1,2,3,4-Cyclobutanetetracarboxylic Acid 1,2,3,4-Tetramethyl Ester is product from the formation of a mixture of maleic anhydride and hexamethylbenzene when exposed to ultraviolet irradiation.
Technology Process of tetramethyl-1,2,3,4-cyclobutanetetracarboxylate

There total 5 articles about tetramethyl-1,2,3,4-cyclobutanetetracarboxylate 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 boron trifluoride; at 65 ℃; for 0.333333h;
DOI:10.1021/ac049919h
Guidance literature:
In water; for 7h; UV-irradiation;
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