Diglycidyl 1,2-cyclohexanedicarboxylate

Base Information

• Chemical Name: Diglycidyl 1,2-cyclohexanedicarboxylate
• CAS No.: 5493-45-8
• Deprecated CAS: 115566-23-9,163516-26-5,163663-42-1,174394-64-0,39403-81-1,65547-06-0,90014-99-6,1234569-31-3,1628271-25-9,1638260-10-2
• Molecular Formula: C14H20O6
• Molecular Weight: 284.309
• Hs Code.: 29172090
• European Community (EC) Number: 226-826-3
• UNII: CD9T07H2IZ
• DSSTox Substance ID: DTXSID7024875
• Nikkaji Number: J75.391B
• Wikidata: Q27275408
• ChEMBL ID: CHEMBL1304981
• Mol file: 5493-45-8.mol

Synonyms:CDCABOM;cyclohexane-1,2-dicarboxylic acid bis(oxiranylmethyl) ester;Epalloy 5200;hexahydrophthalic acid diglycidyl ester

Chemical Property of Diglycidyl 1,2-cyclohexanedicarboxylate

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: n20/D 1.487(lit.)
• Boiling Point: 412.6 °C at 760 mmHg
• Flash Point: 183.3 °C
• PSA: 77.66000
• Density: 1.279 g/cm³
• LogP: 0.67680
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 8
• Exact Mass: 284.12598835
• Heavy Atom Count: 20
• Complexity: 346

Purity/Quality:

98% ^*data from raw suppliers

Diglycidyl 1,2-cyclohexanedicarboxylate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38-43
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CCC(C(C1)C(=O)OCC2CO2)C(=O)OCC3CO3
• Uses: It is used in epoxy-based industrial coatings and paints.

Technology Process of Diglycidyl 1,2-cyclohexanedicarboxylate

There total 1 articles about Diglycidyl 1,2-cyclohexanedicarboxylate 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:

→ trans-Cyclohexan-1,2-dicarbonsaeure-diglycidylester (5493-45-8,25293-69-0,27103-66-8)

Guidance literature:

Umesterung von trans-Cyclohexan-1,2-dicarbonsaeure-dimethylester mit Verb.30, Thallium-Katalysator;

DOI:10.1002/hlca.19770600603

Reference yield:

tetrahydrophthalic acid diglycidyl ester (5493-45-8,27103-66-8) → C14H20O4S2 + C14H20O5S

Guidance literature:

With potassium thioacyanate; In ethanol; water; at 54.84 ℃; for 0.5h; Microwave irradiation;

DOI:10.1007/s10973-015-4527-y