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1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate

Base Information
  • Chemical Name:1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate
  • CAS No.:126812-30-4
  • Molecular Formula:C15H15NO4
  • Molecular Weight:273.288
  • Hs Code.:
  • European Community (EC) Number:847-051-2
  • Nikkaji Number:J3.406.977H
  • Mol file:126812-30-4.mol
1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate

Synonyms:126812-30-4;1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate;2-[(cyclohexylcarbonyl)oxy]-1H-isoindole-1,3(2H)-dione;(1,3-dioxoisoindol-2-yl) cyclohexanecarboxylate;1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl cyclohexanecarboxylate;ChemDiv3_004163;Cambridge id 7029765;SCHEMBL13479740;HMS1484N05;BFA81230;MFCD02189535;STK223456;AKOS001665480;AT20652;IDI1_022073;CS-0216935;EN300-6489204;AN-979/15447008;SR-01000504847;A1-33265;SR-01000504847-1;BRD-K17570253-001-01-0

Suppliers and Price of 1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate
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
  • A1 Biochem Labs
  • 1,3-Dioxoisoindolin-2-ylcyclohexanecarboxylate 95%
  • 2.5 g
  • $ 850.00
Total 6 raw suppliers
Chemical Property of 1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate
Chemical Property:
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:273.10010796
  • Heavy Atom Count:20
  • Complexity:404
Purity/Quality:

99%, *data from raw suppliers

1,3-Dioxoisoindolin-2-ylcyclohexanecarboxylate 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CCC(CC1)C(=O)ON2C(=O)C3=CC=CC=C3C2=O
Technology Process of 1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate

There total 7 articles about 1,3-Dioxoisoindolin-2-yl cyclohexanecarboxylate 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:
Cyclohexanecarboxylic acid; With dmap; dicyclohexyl-carbodiimide; In tetrahydrofuran; for 0.0166667h; Schlenk technique; Inert atmosphere;
N-hydroxyphthalimide; In tetrahydrofuran; at 20 ℃; for 24h; Inert atmosphere; Schlenk technique;
DOI:10.3390/molecules23040764
Guidance literature:
With tert.-butylnitrite; In acetonitrile; at 25 ℃; for 12h; Concentration; Solvent; Catalytic behavior; Inert atmosphere; Schlenk technique; Sealed tube;
DOI:10.1021/acs.orglett.1c03434
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