(Cyclohexylmethyl)benzene

Base Information

• Chemical Name: (Cyclohexylmethyl)benzene
• CAS No.: 4410-75-7
• Molecular Formula: C13H18
• Molecular Weight: 174.286
• Hs Code.: 2902909090
• European Community (EC) Number: 630-605-0
• DSSTox Substance ID: DTXSID00196038
• Nikkaji Number: J62.558B
• Wikidata: Q83069126
• Mol file: 4410-75-7.mol

Synonyms:cyclohexyl-phenyl-methane;benzylcyclohexylmethane;Cyclohexyl-phenyl-methan;benzylcyclohexane;METHANE,CYCLOHEXYLPHENYL;

Chemical Property of (Cyclohexylmethyl)benzene

Chemical Property:

• Vapor Pressure: 0.026mmHg at 25°C
• Boiling Point: 255.6°Cat760mmHg
• Flash Point: 101.5°C
• PSA: 0.00000
• Density: 0.943g/cm³
• LogP: 3.80940
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 174.140850574
• Heavy Atom Count: 13
• Complexity: 127

Purity/Quality:

95% ^*data from raw suppliers

ALPHA-CYCLOHEXYLTOLUENE Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CCC(CC1)CC2=CC=CC=C2

Technology Process of (Cyclohexylmethyl)benzene

There total 76 articles about (Cyclohexylmethyl)benzene 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: 67.0%

Diphenylmethane (101-81-5) → (cyclohexylmethyl)benzene (4410-75-7) + dicyclohexylmethane (3178-23-2)

Guidance literature:

With MmNi_3.5Co_0.7Al_0.8H₄; at 160 ℃; for 3h; under 3677.5 Torr;

DOI:10.1246/cl.1994.431

Reference yield: 55.7%

benzophenone (119-61-9) → Diphenylmethane (101-81-5) + (cyclohexylmethyl)benzene (4410-75-7) + dicyclohexylmethane (3178-23-2)

Guidance literature:

With potassium hydroxide; Raney Ni-Al alloy; In water; at 90 ℃; for 5h;

DOI:10.1080/00397910801929762

Reference yield: 51.6%

1,1-Diphenylmethanol (91-01-0) → Diphenylmethane (101-81-5) + (cyclohexylmethyl)benzene (4410-75-7) + dicyclohexylmethane (3178-23-2)

Guidance literature:

With potassium hydroxide; Raney Ni-Al alloy; In water; at 90 ℃; for 5h;

DOI:10.1080/00397910801929762

upstream raw materials:

1-bromocyclohexane

benzyl sodium

di-tert-butyl peroxide

(1-phenyl-cyclohexyl)-acetaldehyde

Downstream raw materials:

dicyclohexylmethane

3-(4-cyclohexylmethylbenzoyl)acrylic acid

cyclohexyl-(4-nitrophenyl)methane

1-(hydroxy(phenyl)methyl)cyclohexan-1-ol

Refernces

• 1、 Antil, Neha,Kumar, Ajay,Akhtar, Naved,Newar, Rajashree,Begum, Wahida,Manna, Kuntal. "Metal-Organic Framework-Confined Single-Site Base-Metal Catalyst for Chemoselective Hydrodeoxygenation of Carbonyls and Alcohols". supporting information. p. 9029 - 9039. Retrieved 2021/06/28.
• 2、 Ishida, Naoki,Kamae, Yoshiki,Ishizu, Keigo,Kamino, Yuka,Naruse, Hiroshi,Murakami, Masahiro. "Sustainable System for Hydrogenation Exploiting Energy Derived from Solar Light". supporting information. p. 2217 - 2220. Retrieved 2021/02/16.