147838-45-7

Basic information

• Product Name: [1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI)
• Synonyms: [1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI)
• CAS NO: 147838-45-7
• Molecular Formula: C15H16O2
• Molecular Weight: 228.28634
• Product Categories: BIPHENYL
• Mol File: 147838-45-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI)(147838-45-7)
• EPA Substance Registry System: [1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI)(147838-45-7)

Safety Data

• Hazardous Substances Data: 147838-45-7(Hazardous Substances Data)

Usage

General Description

[1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI) is a chemical compound with the molecular formula C19H18O2. It is a derivative of biphenyl, which is a widely used industrial chemical. This specific compound has an ethoxy and methyl group attached to the biphenyl ring, giving it unique properties and potential applications. It may be used in the production of various industrial products or as a starting material in the synthesis of other organic compounds. Its specific uses and properties would depend on its exact chemical and physical characteristics, which would need to be determined through further research and testing.

Upstream product

• 927-80-0 1-ethoxyacetylene 

Relevant articles and documents

A Study of the Reactivity of Tricarbonyl(vinylketene)iron(0) Complexes Towards Alkynes

Alkynes add to tricarbonyl(vinylketene)iron(0) complexes to generate stable 1:1 adducts, the structures of which were determined by an X-ray crystal structure analysis of the adduct formed from tricarbonyl(5-phenyl-3-iso-propyl-1-oxapenta-1,2,4-triene)iron(0) and dimethyl acetylenedicarboxylate.Addition of unsymmetrical alkynes is regioselective and the regiochemistries of the adducts isolated from these reactions were determined by X-ray crystal structure analyses of the products from but-3-yn-2-one and tricarbonyl(3-tert-butyl-5-phenyl-1-oxapenta-1,2,4-triene)iron(0), and of the structurally modified product derived from diethylpropynylamine and tricarbonyl(5-phenyl-3-iso-propyl-1-oxapenta-1,2,4-triene)iron(0).Thermolysis of the adducts leads to either cyclopentenediones or phenols and its outcome is dependent on the electronic properties of the carbon-1 substituent of the adduct.The phenols may be synthesised directly and regioselectively from tricarbonyl(vinylketene)iron(0) complexes and the appropriate alkynes.