6954-45-6

Basic information

• Product Name: (2-CHLORO-PHENYL)-PHENYL-METHANOL
• Synonyms: (2-CHLORO-PHENYL)-PHENYL-METHANOL;AURORA KA-7059;o-Chlorobenzhydrol;α-(o-Chlorophenyl)benzyl alcohol;α-Phenyl-2-chlorobenzenemethanol;Nsc37575
• CAS NO: 6954-45-6
• Molecular Formula: C₁₃H₁₁ClO
• Molecular Weight: 218.68
• Mol File: 6954-45-6.mol
• Article Data: 54

Chemical Properties

• Boiling Point: 344.1 ºC at 760 mmHg
• Flash Point: 161.9 ºC
• Appearance: /
• Density: 1.221 g/cm³
• Vapor Pressure: 2.57E-05mmHg at 25°C
• Refractive Index: 1.609
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (2-CHLORO-PHENYL)-PHENYL-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (2-CHLORO-PHENYL)-PHENYL-METHANOL(6954-45-6)
• EPA Substance Registry System: (2-CHLORO-PHENYL)-PHENYL-METHANOL(6954-45-6)

Safety Data

• Hazardous Substances Data: 6954-45-6(Hazardous Substances Data)

Usage

General Description

"(2-Chloro-Phenyl)-Phenyl-Methanol" is a chemical compound that consists of a phenyl and a methanol group on a phenyl ring which features a chlorine substitute at the second carbon atom. It is a derivative of benzene and an alcohol, making it an aromatic compound with hydrophilic properties. As a complex organic compound, its potential uses may vary across several industries including pharmaceuticals, synthesis of other chemicals, and materials science. However, specific details such as the chemical reaction it may undergo or the properties that it displays would be determined by the context in which it is used. Like many chemicals, it requires careful handling and usage due to possible risks associated with the chlorine group.

InChI:InChI=1/C13H11ClO/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-9,13,15H

Upstream product

• 5162-03-8 (2-chlorophenyl)(phenyl)methanone 
• 89-98-5 2-chloro-benzaldehyde 
• 95950-06-4 1,2-bis-(2-chloro-phenyl)-1,2-diphenyl-ethane-1,2-diol 
• 108-38-3 m-xylene 
• 109-72-8 n-butyllithium 
• 17051-75-1 o-chlorophenyl phenyl sulfoxide 
• 100-52-7 benzaldehyde 
• 15842-76-9 (2-chloro-phenyl)-trimethyl-silane 
• 76847-21-7 2-Chlor-1-benzol 
• 64-17-5 ethanol 
• 615-41-8 2-iodochlorobenzene 
• 934-56-5 trimethyl(phenyl)stannane 
• 98-80-6 phenylboronic acid 
• 100-58-3 phenylmagnesium bromide 

Downstream Products

• 29921-41-3 (o-benzyl)chlorobenzene 
• 56961-47-8 2-chloro-benzhydryl chloride 
• 76847-21-7 2-Chlor-1-benzol 
• 574-42-5 benzhydryl ether 
• 136908-12-8 1-(Benzhydryloxy-phenyl-methyl)-2-chloro-benzene 
• 136908-25-3 C₂₆H₂₀Cl₂O 
• 136908-26-4 1,1'-(1,1'-oxybis(ethane-1,1-diyl))dinaphthalene 
• 136908-13-9 1-{1-[(2-Chloro-phenyl)-phenyl-methoxy]-ethyl}-naphthalene 
• 75341-34-3 (2-chlorophenyl)phenylbromomethane 
• 7732-18-5 water 
• 1509911-88-9 (E)-(3-(2-chlorophenyl)prop-1-ene-1,3-diyl)dibenzene 
• 16071-25-3 (S)-2-chlorobenzhydrol 

Relevant articles and documents

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Transition-metal catalysts are powerful tools for carbon-carbon bond-forming reactions that are difficult to achieve using native enzymes. Enzymes that exhibit inherent selectivities and reactivities through host-guest interactions have inspired widesprea

4-Methyltetrahydropyran (4-MeTHP): Application as an Organic Reaction Solvent

4-Methyltetrahydropyran (4-MeTHP) is a hydrophobic cyclic ether with potential for industrial applications. We herein report, for the first time, a comprehensive study on the performance of 4-MeTHP as an organic reaction solvent. Its broad application to organic reactions includes radical, Grignard, Wittig, organometallic, halogen-metal exchange, reduction, oxidation, epoxidation, amidation, esterification, metathesis, and other miscellaneous organic reactions. This breadth suggests 4-MeTHP can serve as a substitute for conventional ethers and harmful halogenated solvents. However, 4-MeTHP was found incompatible with strong Lewis acids, and the C?O bond was readily cleaved by treatment with BBr3. Moreover, the radical-based degradation pathways of 4-MeTHP, THP and 2-MeTHF were elucidated on the basis of GC-MS analyses. The data reported herein is anticipated to be useful for a broad range of synthetic chemists, especially industrial process chemists, when selecting the reaction solvent with green chemistry perspectives.

Diaryl hydroxylamines as pan or dual inhibitors of indoleamine 2,3-dioxygenase-1, indoleamine 2,3-dioxygenase-2 and tryptophan dioxygenase

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