6196-94-7

Basic information

• Product Name: 1-(4-Ethylphenyl)-1-phenylethane
• Synonyms: 1-(4-Ethylphenyl)-1-phenylethane;1-Ethyl-4-(1-phenylethyl)benzene
• CAS NO: 6196-94-7
• Molecular Formula: C₁₆H₁₈
• Molecular Weight: 210.31
• Mol File: 6196-94-7.mol
• Article Data: 9

Chemical Properties

• Melting Point: -62 °C
• Boiling Point: 303.1 °C at 760 mmHg
• Flash Point: 140.5 °C
• Appearance: /
• Density: 0.96 g/cm³
• Vapor Pressure: 0.0017mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: 1-(4-Ethylphenyl)-1-phenylethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Ethylphenyl)-1-phenylethane(6196-94-7)
• EPA Substance Registry System: 1-(4-Ethylphenyl)-1-phenylethane(6196-94-7)

Safety Data

• Hazardous Substances Data: 6196-94-7(Hazardous Substances Data)

Usage

Description

1-(4-Ethylphenyl)-1-phenylethane, also known as ethylbenzylbenzene, is a colorless liquid chemical compound with the molecular formula C20H20. It is insoluble in water and has a slightly sweet, floral odor.

Uses

Used in Fragrance and Flavor Industry:
1-(4-Ethylphenyl)-1-phenylethane is used as a fragrance and flavoring agent for its slightly sweet, floral odor in various consumer products such as perfumes, colognes, and food additives.
Used in Chemical Synthesis:
1-(4-Ethylphenyl)-1-phenylethane is used as a solvent and a starting material for the synthesis of other organic compounds.
Used in Pharmaceutical Research:
1-(4-Ethylphenyl)-1-phenylethane has been studied for its potential use as an anti-inflammatory and antitumor agent, although further research is needed to confirm its efficacy and safety.
Safety Precautions:
It is important to handle 1-(4-Ethylphenyl)-1-phenylethane with care, as it can be harmful if inhaled, ingested, or comes into contact with the skin.

InChI:InChI=1/C16H18/c1-3-14-9-11-16(12-10-14)13(2)15-7-5-4-6-8-15/h4-13H,3H2,1-2H3

Upstream product

• 1585-07-5 1-bromo-4-ethylbenzene 
• 585-71-7 (1-bromoethyl)benzne 
• 100-41-4 ethylbenzene 
• 98-85-1 1-Phenylethanol 
• 93-92-5 1-phenylethyl acetate 
• 937-30-4 4-ethylacetophenone 
• 492-37-5 hydratropic acid 
• 275-03-6 tetrazolo[1,5-a]pyrimidine 
• 110-82-7 cyclohexane 
• 41453-02-5 NbMe₂Cl₃ 
• 100-52-7 benzaldehyde 
• 234-41-3 naphtho[1,2-b]thiophene 
• 100-42-5 styrene 
• 77989-25-4 1-(4-ethyl-phenyl)-1-phenyl-ethene 

Downstream Products

• 93015-22-6 1-(4-ethyl-phenyl)-1-phenyl-ethyl hydroperoxide 
• 123-07-9 4-Ethylphenol 
• 98-86-2 acetophenone 
• 611-95-0 4-carboxybenzophenone 

Relevant articles and documents

Continuous synthesis of organozinc halides coupled to Negishi reactions

The Negishi cross-coupling is a powerful C-C bond forming reaction. The method is less commonly used relative to other cross-coupling methods in part due to lack of availability of organozinc species. While organozinc species can be prepared, problems wit

Selective one-pot synthesis of various phenols from diarylethanes

Various substituted phenols were selectively synthesized by a one-pot reaction through the NHPI-catalyzed aerobic oxidation of 1,1-diarylethanes followed by treatment with dilute sulfuric acid. The Royal Society of Chemistry.

Selective arylation of exocyclic N-position of 2-pyrimidylnitrenium ion photolytically generated from tetrazolo[1,5-a]pyrimidine in the presence of trifluoroacetic acid

Photo-reactions of tetrazolo[1,5-a]pyrimidine (1) with benzene (2a) and substituted benzenes (2b-f) in the presence of trifluoroacetic acid (TFA) gave 2-(2-, 3- and 4-substituted anilino)pyrimidines (3-5) together with 2-aminopyridine (6) and biphenyl (7) or diarylmethanes (8b, 8c and 8e). From the effect of heavy-atom solvent on the reactions, it is reasonable to assume that 3-5 are formed via a singlet species, but 6-8 via a triplet species. The intermediacy of 2-pyrimidylnitrenium ion is consistent with the evidence derived by the above effect, by a Hammett plot with p = -2.9 and by effects of solvent nucleophilicity and counter-anions. The selective exocyclic N-arylation giving 3-5 is discussed.