Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-

Base Information

• Chemical Name: Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-
• CAS No.: 13446-84-9
• Molecular Formula: C₂₄H₂₈O₄
• Molecular Weight: 380.484
• European Community (EC) Number: 810-464-3
• DSSTox Substance ID: DTXSID201019606
• Nikkaji Number: J2.789.355D
• Mol file: 13446-84-9.mol

Synonyms:13446-84-9;Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-;SCHEMBL5598711;DTXSID201019606;AS-84848;NS00134102;E85594;2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-Oxirane;2,2'-[CYCLOHEXYLIDENEBIS(4,1-PHENYLENEOXYMETHYLENE)]BIS[OXIRANE];2-[[4-[1-[4-(oxiran-2-ylmethoxy)phenyl]cyclohexyl]phenoxy]methyl]oxirane;2,2'-(((Cyclohexane-1,1-diylbis(4,1-phenylene))bis(oxy))bis(methylene))bis(oxirane);2-{[4-(1-{4-[(oxiran-2-yl)methoxy]phenyl}cyclohexyl)phenoxy]methyl}oxirane

Chemical Property of Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-

Chemical Property:

• Density: 1.116g/cm3 at 23℃
• XLogP3: 5.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 8
• Exact Mass: 380.19875937
• Heavy Atom Count: 28
• Complexity: 449

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CCC(CC1)(C2=CC=C(C=C2)OCC3CO3)C4=CC=C(C=C4)OCC5CO5

Technology Process of Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis-

There total 3 articles about Oxirane, 2,2'-[cyclohexylidenebis(4,1-phenyleneoxymethylene)]bis- 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: 90.0%

1,1-bis(p-hydroxyphenyl)cyclohexane (843-55-0) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → bisphenol Z diglycidyl ether (13446-84-9)

Guidance literature:

With sodium hydroxide; In isopropyl alcohol; at 70 ℃; for 0.333333h;

DOI:10.1080/10587250008023599

Reference yield:

cyclohexanone (108-94-1,11119-77-0,9003-41-2,9075-99-4) → bisphenol Z diglycidyl ether (13446-84-9)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. HCl; mercaptopropionic acid / 30 h / 25 - 50 °C

2: 90 percent / aq. NaOH / propan-2-ol / 0.33 h / 70 °C

With hydrogenchloride; sodium hydroxide; 2-mercaptopropanoic acid; In isopropyl alcohol;

DOI:10.1080/10587250008023599

Reference yield:

phenol (108-95-2,27073-41-2) → bisphenol Z diglycidyl ether (13446-84-9)

Guidance literature:

Multi-step reaction with 2 steps

1: aq. HCl; mercaptopropionic acid / 30 h / 25 - 50 °C

2: 90 percent / aq. NaOH / propan-2-ol / 0.33 h / 70 °C

With hydrogenchloride; sodium hydroxide; 2-mercaptopropanoic acid; In isopropyl alcohol;

DOI:10.1080/10587250008023599

upstream raw materials:

1,1-bis(p-hydroxyphenyl)cyclohexane

epichlorohydrin

cyclohexanone

phenol

Downstream raw materials:

1,1-bis[4-(3-methacryloyloxy-2-hydroxypropoxy)phenyl]cyclohexane

C₂₄H₃₀Cl₂O₄

1,1-bis[4-(3-acryloyloxy-2-hydroxypropoxy)phenyl]cyclohexane