4404-61-9

Basic information

• Product Name: cyclohexyl(diphenyl)methanol
• Synonyms: benzenemethanol, alpha-cyclohexyl-alpha-phenyl-; Diphenyl-cyclohexyl-methanol
• CAS NO: 4404-61-9
• Molecular Formula: C₁₉H₂₂O
• Molecular Weight: 266.3774
• Mol File: 4404-61-9.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 414.2°C at 760 mmHg
• Flash Point: 162.8°C
• Density: 1.081g/cm³
• Vapor Pressure: 1.33E-07mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: cyclohexyl(diphenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: cyclohexyl(diphenyl)methanol(4404-61-9)
• EPA Substance Registry System: cyclohexyl(diphenyl)methanol(4404-61-9)

Safety Data

• Hazardous Substances Data: 4404-61-9(Hazardous Substances Data)

Usage

General Description

Cyclohexyl(diphenyl)methanol is a chemical compound with the molecular formula C19H22O. It is commonly used as a fragrance ingredient in perfumes and personal care products due to its pleasant aromatic properties. It is a white solid at room temperature with a slightly sweet, floral odor. It is also used as a solvent and a chemical intermediate in the production of other organic compounds. The chemical structure of cyclohexyl(diphenyl)methanol contains a cyclohexyl ring and two phenyl groups, which contribute to its unique fragrance and chemical properties. It is important to handle this chemical with care and follow safety guidelines due to its potential to cause skin and eye irritation.

Upstream product

• 119-61-9 benzophenone 
• 931-51-1 cyclohexylmagnesiumchloride 
• 16491-63-7 cyclohexanecarboxylic acid allyl ester 
• 3289-28-9 ethyl cyclohexanecarboxylate 
• 16002-63-4 phenylmagnesium iodide 
• 712-50-5 Cyclohexyl phenyl ketone 
• 110-82-7 cyclohexane 
• 591-50-4 iodobenzene 
• 72399-18-9 formaldehyde O-benzyloxime 
• 629-27-6 1-Iodooctane 
• 4786-20-3 crotononitrile 
• 626-62-0 Cyclohexyl iodide 
• 623-43-8 crotonic acid methyl ester 
• 153094-32-7 O,O'-bistributyltin benzopinacolate 

Downstream Products

• 30125-24-7 1,1-diphenylmethylenecyclohexane 
• 50585-08-5 (cyclohexylmethylene)dibenzene 
• 102176-79-4 chloro-cyclohexyl-diphenyl-methane 
• 1016565-40-4 C₂₂H₂₇NO₂S 

Relevant articles and documents

Persistent room temperature blue phosphorescence from racemic crystals of 1,1-diphenylmethanol derivatives

Among the six alkyldiphenylmethanol derivatives assessed in this study, five showed persistent room temperature phosphorescence (pRTP), whereas the original diphenylmethanol (DPhHOH) did not. pRTP is a unique luminescence phenomenon that appears only in t

Synthesis and application of 2,6-bis(trifluoromethyl)-4-pyridyl phosphanes: The most electron-poor aryl phosphanes with moderate bulkiness

The poor will be rich: BFPy phosphanes (see scheme) mimic the electronic and steric characters of P(C6F5)3 and PPh 3, respectively. These novel ligands showed a large ligand acceleration effect on Stille coupling, the Rh-catalyzed 1,2-addition of aryl boronic acid to unactivated ketones and the asymmetric arylation of N-tosylimine using phenylboronic acid. Copyright

Triaryl methane derivatives as antiproliferative agents

Clotrimazole (CLT) 1, a synthetic anti-fungal imidazole derivative, inhibits tumor cell proliferation and angiogenesis. In the current study, flow cytometric analysis demonstrated that the decrease in tumor cell growth by CLT 1 was associated with inhibition of cell cycle progression at the G 1-S phase transition, resulting in G0-G1 arrest. A series of CLT 1 analogues has been generated in order to develop CLT 1 derivatives that are devoid of the imidazole moiety which is responsible for the hepatoxicity associated with CLT 1 while retaining CLT 1 efficacy. The majority of these analogues demonstrate in vitro antiproliferative activity ranging from submicromolar to micromolar concentrations.