Synonyms: "p-cyclohexylphenol", "4-hydroxyphenylcyclohexane"

Source: 4-cyclohexylphenol is used in the formation of resin.


IUPAC Name: 4-cyclohexylphenol
CAS Number: 1131-60-8
PubChem ID: 14327
Canonical SMILES: C1CCC(CC1)C2=CC=C(C=C2)O

Structural Properties:

Molecular Formula: C12H16O
Molecular Weight: 176,2548

Pharmacophore Features:

Number of bond donors: 1
Number of bond acceptors: 1
Number of atoms different from hydrogen: 13


2D structure (.sdf)
3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)

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Toxicological Information

ACToR (Aggregated Computational Toxicology Resource)

Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Akahori Y, Nakai M, Yamasaki K, Takatsuki M, Shimohigashi Y, Ohtaki M. 2008. Relationship between the results of in vitro receptor binding assay to human estrogen receptor alpha and in vivo uterotrophic assay: Comparative study with 65 selected chemicals. Toxicol in Vitro 22(1):225-231.
Ogawa Y, Kawamura Y, Wakui C, Mutsuga M, Nishimura T, Tanamoto K. 2006. Estrogenic activities of chemicals related to food contact plastics and rubbers tested by the yeast two-hybrid assay. Food Additives & Contaminants 23(4):422-430.
Yamasaki K, Takeyoshi M, Sawaki M, Imatanaka N, Shinoda K, Takatsuki M. 2003. Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals. Toxicology 183(1-3):93-115.

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