3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate

Base Information

• Chemical Name: 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate
• CAS No.: 25085-98-7
• Deprecated CAS: 37042-87-8,1403253-45-1,1403490-03-8,1872260-35-9,11120-79-9,111483-58-0,129773-39-3,30350-17-5,39354-66-0,50809-37-5,50861-60-4,52725-58-3,61489-54-1,65430-69-5,9083-95-8,95078-14-1,121396-47-2,125053-37-4,137607-28-4,146123-76-4,189201-55-6,216496-08-1,251369-29-6,299423-35-1,620963-33-9,889878-13-1,95078-13-0,1003891-93-7,1298077-19-6,1312673-06-5,939768-34-0,1809950-19-3,1865698-96-9,1872260-36-0,2007107-18-6,1704062-10-1,2009012-09-1,1461703-61-6,2173329-14-9
• Molecular Formula: (C14H20O4)x
• Molecular Weight: 0
• European Community (EC) Number: 219-207-4,609-326-3,687-470-6
• UNII: S224DEL3P4
• DSSTox Substance ID: DTXSID2027466
• Nikkaji Number: J42.541I
• Wikipedia: 3,4-Epoxycyclohexylmethyl-3%27,4%27-epoxycyclohexane_carboxylate
• Wikidata: Q19694494
• ChEMBL ID: CHEMBL2143072
• Mol file: 25085-98-7.mol

Synonyms:2386-87-0;3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate;7-Oxabicyclo[4.1.0]heptan-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate;Chissonox 221 monomer;ERL-4221;UT-632;3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexane carboxylate;3,4-EPOXYCYCLOHEXYLMETHYL-3,4-EPOXYCYCLOHEXANECARBOXYLATE;DTXSID2027466;HSDB 5873;3,4-Epoxycyclohexanecarboxylic acid (3,4-epoxycyclohexylmethyl) ester;(3,4-Epoxycyclohexyl)methyl 3,4-epoxycyclohexylcarboxylate;EINECS 219-207-4;UT 632;BRN 1381750;UNII-S224DEL3P4;CCRIS 8882;S224DEL3P4;7-Oxabicyclo(4.1.0)heptane-3-carboxylic acid, 7-oxabicyclo(4.1.0)hept-3-ylmethyl ester;7-Oxabicyclo[4.1.0]heptane-3-carboxylic acid, 7-oxabicyclo[4.1.0]hept-3-ylmethyl ester;3,4-Epoxycyclohexanemethyl 3,4-epoxycyclohexanecarboxylate;7-Oxabicyclo(4.1.0)hept-3-ylmethyl 7-oxabicyclo(4.1.0)heptane-3-carboxylate;EC 219-207-4;DTXCID707466;7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate;ECC;CAS-2386-87-0;3,4-epoxycyclohexylmethyl3,4-epoxycyclo-hexaneca;SCHEMBL24975;UVA 1500 MONOMER;CHEMBL2143072;BCP32770;CEL-2021;Ctcloaliphatic epoxy resin UP-632;Tox21_202388;Tox21_303312;MFCD00440900;UP-632;AKOS015915254;CS-W012617;NCGC00164163-01;NCGC00164163-02;NCGC00256981-01;NCGC00259937-01;AS-17792;LS-98670;FT-0651573;F16450;A816945;W-107371;Q19694494;3,4-?Epoxycyclohexylmethyl 3,4-?epoxycyclohexanecarboxylate;3,4-epoxycyclohexylmethyl (3,4-epoxy)cyclohexanecarboxylate;3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexanecarboxylate;3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate;3,4-?Epoxycyclohexylmethyl 3,4-?epoxycyclohexanecarboxylate, 97%;3,4-EPOXYCYCLOHEXANEMETHYL 3,4-EPOXYCYCLOHEXANECARBOXYLATE [HSDB];7-OXABICYCLO(4.1.0)HEPT-3-YLMETHYL 7- OXABICYCLO(4.1.0)HEPTANE-3-CARBOXYLATE;7-Oxabicyclo[4.1.0]hept-3-ylmethyl 7-oxabicyclo[4.1.0]heptane-3-carboxylate #;7-oxabicyclo[4.1.0]hept-3-ylmethyl7-oxabicyclo[4.1.0]heptane-3-carboxylate;25085-98-7;7-OXABICYCLO[4.1.0]HEPTANE-3-CARBOXYLIC ACID,7-OXABICYCLO[4.1.0]HEPT-3-YLMETHYL ESTER

Chemical Property of 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate

Chemical Property:

• XLogP3: 1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 252.13615911
• Heavy Atom Count: 18
• Complexity: 356

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Plastics & Rubber -> Glycidyl Ethers
• Canonical SMILES: C1CC2C(O2)CC1COC(=O)C3CCC4C(C3)O4
• Recent ClinicalTrials: Metastatic Gastric Cancer FFCD 03-07

Technology Process of 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate

There total 1 articles about 3,4-Epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate 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: 94.0%

3-cyclohexene-1-carboxylic acid 3-cyclohexen-1-ylmethyl ester (2611-00-9) → 3,4-epoxycyclohexylmethyl 3,4-epoxycyclohexanecarboxylate (2386-87-0,25085-98-7,37042-87-8)

Guidance literature:

With phosphotungstic acid; trioctylmethylammonium acetate; phosphoric acid; dihydrogen peroxide; sodium carbonate; In water; toluene; at 50 ℃; for 15h; Inert atmosphere;

upstream raw materials:

3-cyclohexene-1-carboxylic acid 3-cyclohexen-1-ylmethyl ester