6624-06-2

Basic information

• Product Name: 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran
• CAS NO: 6624-06-2
• Molecular Formula: C₃₂H₂₄O
• Molecular Weight: 424.5324
• Mol File: 6624-06-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 545.1°C at 760 mmHg
• Flash Point: 262°C
• Density: 1.168g/cm³
• Vapor Pressure: 2.19E-11mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran(6624-06-2)
• EPA Substance Registry System: 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran(6624-06-2)

Safety Data

• Hazardous Substances Data: 6624-06-2(Hazardous Substances Data)

Usage

Type of compound

Dihydrobenzofuran derivative

Explanation

A dihydrobenzofuran derivative is a cyclic ether that contains both a benzene ring and a furan ring. The presence of these two rings gives the compound unique chemical properties.

Explanation

The compound's structure and properties make it useful in various fields, including the creation of new organic compounds, development of materials with specific properties, and research into potential pharmaceutical applications.

Explanation

The compound appears as a white, crystalline solid, which is a common form for many organic compounds.

Explanation

The molecular weight is the mass of one mole of a substance, calculated by adding the atomic weights of all the atoms in the molecule. In this case, the molecular weight of 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran is 450.56 grams per mole.

Explanation

The structure of 1,1,3,3-tetraphenyl-1,3-dihydro-2-benzofuran allows it to interact with other molecules, which can lead to the formation of new compounds with unique and potentially valuable properties.

Applications

Organic synthesis, materials science, and pharmaceutical research

Physical state

White crystalline solid

Molecular weight

450.56 g/mol

Interaction with other molecules

Potential for creating new compounds with interesting properties

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Downstream Products

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Relevant articles and documents

The Pyrolyses of 1,1,4,4-Tetraphenyl-1,4-butanediol and 1,1,4,4-Tetraphenyl-2-butene-1,4-diol Derivatives. Decomposition Reactions to Form Olefins via the Elimination of Two Mole Equivalents of the Hydroxydiphenylmethyl Radical

The pyrolysis of 1,1,2,4,4-pentaphenyl-1,4-butandiol, trans-1,2-bis(hydroxydiphenylmethyl)hexane, trans-1,2-bis(hydroxydiphenylmethyl)indan, and cis-endo- and trans-1,2-bis(hydroxydiphenylmethyl)bicycloheptane gave styrene, cyclohexene, indene, and norbornene respectively, accompanied by benzophenone and benzhydrol.The pyrolysis of trans-1,2-bis(hydroxydiphenylmethyl)spironona-4,6,8-triene afforded indene via rearrangement to form trans-1,2-bis(hydroxydiphenylmethyl)indan.The pyrolysis of cis-1,1,4,4-tetraphenyl-2-butene-1,4-diol afforded 2,2,5,5-tetraphenyl-2,5-dihydrofuran.On the other hand, trans-1,1,4,4-tetraphenyl-2- butene-1,4-diol afforded 1,2,4,4-tetraphenyl-3-buten-1-one.The mechanisms of these decomposition reactions are discussed.