1,1-Bis(4-hydroxyphenyl)cyclopentane

Base Information

• Chemical Name: 1,1-Bis(4-hydroxyphenyl)cyclopentane
• CAS No.: 788-57-8
• Molecular Formula: C17H18O2
• Molecular Weight: 254.329
• NSC Number: 663987,59802
• DSSTox Substance ID: DTXSID90229309
• Nikkaji Number: J77.934B
• Wikidata: Q83109531
• ChEMBL ID: CHEMBL1208076
• Mol file: 788-57-8.mol

Synonyms:788-57-8;4-[1-(4-hydroxyphenyl)cyclopentyl]phenol;1,1-Bis(4-hydroxyphenyl)cyclopentane;1,1-Cyclopentanediphenol;Phenol, 4,4'-cyclopentylidenedi-;Phenol, 4,4'-cyclopentylidenebis-;NSC 59802;BRN 1979007;NSC663987;4,4'-(cyclopentane-1,1-diyl)diphenol;3-06-00-05613 (Beilstein Handbook Reference);NSC59802;Enamine_000545;NCIOpen2_002480;Oprea1_315629;Oprea1_854901;4,4'-cyclopentylidenediphenol;SCHEMBL120895;CHEMBL1208076;DTXSID90229309;MFCD00019288;NSC-59802;ZINC00235823;4,4'-cyclopentane-1,1-diyldiphenol;AKOS001012705;NSC-663987;NCGC00338546-01;LS-104292;AB01330804-02;EN300-18212043;Z56766912;F0020-1563

Chemical Property of 1,1-Bis(4-hydroxyphenyl)cyclopentane

Chemical Property:

• Boiling Point: 427.8°Cat760mmHg
• Flash Point: 203.4°C
• Density: 1.197g/cm³
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 254.130679813
• Heavy Atom Count: 19
• Complexity: 256

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCC(C1)(C2=CC=C(C=C2)O)C3=CC=C(C=C3)O

Technology Process of 1,1-Bis(4-hydroxyphenyl)cyclopentane

There total 6 articles about 1,1-Bis(4-hydroxyphenyl)cyclopentane 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: 100.0%

→ 1,1-bis(p-hydroxyphenyl)cyclopentane (788-57-8)

Guidance literature:

Reference yield: 90.0%

cyclopentanone (120-92-3) + phenol (108-95-2,27073-41-2) → 1,1-bis(p-hydroxyphenyl)cyclopentane (788-57-8)

Guidance literature:

With hydrogenchloride; cetyltrimethylammonium chloride; 3-mercaptopropionic acid; sodium hydroxide; In water; for 4h;

Reference yield:

phenol (108-95-2,27073-41-2) → 1,1-bis(p-hydroxyphenyl)cyclopentane (788-57-8)

Guidance literature:

Multi-step reaction with 3 steps

1: phosphoric acid / toluene / 2 h

2: bis(benzonitrile)palladium(II) dichloride / toluene / 2 h / 130 - 150 °C

3: hydrogenchloride / water / 24 h / 80 °C

With hydrogenchloride; bis(benzonitrile)palladium(II) dichloride; phosphoric acid; In water; toluene;

upstream raw materials:

cyclopentanone

phenol

hydrogenchloride

cyclopenta-1,3-diene

Downstream raw materials:

4-cyclopentylphenol

phenol

1,1-bis[4-(4-nitrophenoxy)phenyl]cyclopentane

1,1-bis[4-(4-nitro-2-trifluoromethylphenoxy)phenyl]cyclopentane

Refernces

• 1、 -. "METHOD OF PRODUCING FIVE-CARBON RING-CONTAINING COMPOUND AND FIVE-CARBON RING DERIVATIVE-CONTAINING POLYURETHANE, AND FIVE-CARBON RING DERIVATIVE-CONTAINING POLYURETHANE". . . Retrieved 2019/02/24.
• 2、 Wang, Xuemei,Liu, Feng,Lai, Jiancheng,Fu, Zhiqiang,You, Xiaozeng. "Comparative investigations on the effects of pendent trifluoromethyl group to the properties of the polyimides containing diphenyl-substituted cyclopentyl Cardo-structure". . p. 27 - 37. Retrieved 2014/06/24.