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

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

Uses

Used in Chemical Synthesis:
[1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI) is used as a starting material for the synthesis of other organic compounds due to its unique functional groups and structural features.
Used in Industrial Production:
[1,1-Biphenyl]-4-ol,2-ethoxy-5-methyl-(9CI) may be utilized in the production of various industrial products, taking advantage of its specific chemical and physical properties.

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.

Conversion of Adducts formed from Tricarbonyl(vinylketene)iron(0) Complexes and Alkynes into Cyclopentenediones and Phenols

Thermolysis of adducts formed from tricarbonyl(vinylketene)iron(0) complexes and alkynes leads to either cyclopentenediones or phenols and its outcome is controlled by the electronic properties of the C-1 substituent of the adduct; the phenols may be synt