17755-10-1

Basic information

• Product Name: [1,1-Biphenyl]-2-ol,3-methyl-(9CI)
• Synonyms: [1,1-Biphenyl]-2-ol,3-methyl-(9CI);2-(3-Methylphenyl)phenol;2-Methyl-6-phenylphenol;3-Methylbiphenyl-2-ol;1,1-Biphenyl]-2-ol, 3-Methyl
• CAS NO: 17755-10-1
• Molecular Formula: C₁₃H₁₂O
• Molecular Weight: 184.23
• Product Categories: BIPHENYL
• Mol File: 17755-10-1.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 295.489°C at 760 mmHg
• Flash Point: 139.714°C
• Appearance: /
• Density: 1.087
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.595
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: [1,1-Biphenyl]-2-ol,3-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1-Biphenyl]-2-ol,3-methyl-(9CI)(17755-10-1)
• EPA Substance Registry System: [1,1-Biphenyl]-2-ol,3-methyl-(9CI)(17755-10-1)

Safety Data

• Hazardous Substances Data: 17755-10-1(Hazardous Substances Data)

Usage

General Description

[1,1-Biphenyl]-2-ol,3-methyl-(9CI) is a chemical compound with the molecular formula C14H12O. It is a derivative of biphenyl, a type of aromatic hydrocarbon. [1,1-Biphenyl]-2-ol,3-methyl-(9CI) contains a hydroxyl group (OH) attached to a methyl group on the biphenyl ring. The compound is used in various chemical reactions and organic synthesis processes, and it may have potential applications as a building block in the production of other chemicals. Additionally, it may exhibit certain biological activities or properties, although further research is needed to fully understand its potential uses and effects.

InChI:InChI=1/C13H12O/c1-10-6-5-9-12(13(10)14)11-7-3-2-4-8-11/h2-9,14H,1H3

Upstream product

• 72569-05-2 ortho-methylphenyl pivalate 
• 66003-76-7 Diphenyliodonium triflate 
• 201230-82-2 carbon monoxide 
• 95-48-7 ortho-cresol 
• 144930-50-7 mesityl(phenyl)iodonium triflouromethanesulfonate 
• 591-50-4 iodobenzene 
• 4783-78-2 2-(o-tolyloxy)pyridine 
• 98-80-6 phenylboronic acid 
• 1033783-02-6 potassium (2-hydroxy-3-methylphenyl)trifluoroborate 
• 23657-53-6 4-methyldibenzo[b,d]thiophene 5,5-dioxide 
• 7372-88-5 4-methyldibenzothiophene 
• 1100054-83-8 6-methylene-2-phenyl-2-cyclohexen-1-one 
• 304-06-3 3-phenylsalicylic acid 
• 13319-71-6 2-bromo-6-methylphenol 

Downstream Products

• 22040-03-5 2-Methyl-6-phenyl-phenylether 
• 1258268-39-1 C₁₆H₁₁Cl₂N₃O 
• 21389-91-3 2-<2-Methyl-6-phenylphenoxy>-aethyl-diaethylamin 
• 17361-99-8 4-bromo-6-methyl-2-phenylphenol 
• 22040-08-0 O-3-benzylbiphenyl-2-ol 

Relevant articles and documents

A Facile Synthesis of the Unsymmetrically Methyl-Substituted 2-Hydroxybiphenyls by Regioselective Cleavage of Dibenzofuran Derivatives with Lithium Metal

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Palladium-Catalyzed Reductive [5+1] Cycloaddition of 3-Acetoxy-1,4-enynes with CO: Access to Phenols Enabled by Hydrosilanes

A new palladium-catalyzed reductive [5+1] cycloaddition of 3-acetoxy-1,4-enynes with CO, enabled by hydrosilanes, has been developed for delivering valuable functionalized phenols. This methodology employs hydrosilanes as the external reagent to facilitate the [5+1] carbonylative benzannulation. The reaction is a conceptually and mechanistically novel carbonylative cycloaddition route for the construction of substituted phenols, through the formation of four new chemical bonds, with excellent functional-group tolerance.

Stoichiometric to catalytic reactivity of the aryl cycloaurated species with arylboronic acids: Insight into the mechanism of gold-catalyzed oxidative C(sp2)-H arylation

Based on the well-defined five-membered aryl gold(iii) complexes, [Au(tpy)X2] (3a and 3b) and [AuBr(Ph)(tpy)] (7), as well as the aryl gold(iii) complex [AuCl2(Ph)(tpy)] (8) (tpy = 2-(o-tolyl)pyridine) as reliable models, we present a detailed study of the mechanism for gold(iii)-catalyzed oxidative cross-coupling reactions between cycloaurable arenes and arylboronic acids. Here we report the direct evidence for a mechanistic proposal including arene C-H activation, transmetallation and biaryl reductive elimination. The chelation-assisted C-H activation strategy has been used for the development of the gold(iii)-catalyzed C-H bond arylation of arenes with aryl reagents to forge extended π-conjugated systems. This journal is