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

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

Uses

Used in Pharmaceutical Industry:
(2-Chloro-Phenyl)-Phenyl-Methanol is used as an intermediate compound for the synthesis of pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, potentially contributing to the treatment of various medical conditions.
Used in Chemical Synthesis:
In the field of chemical synthesis, (2-Chloro-Phenyl)-Phenyl-Methanol is used as a building block for the creation of other complex organic compounds. Its reactivity and structural features make it a valuable precursor in the production of specialty chemicals and materials.
Used in Materials Science:
(2-Chloro-Phenyl)-Phenyl-Methanol is utilized in materials science for the development of novel materials with specific properties. Its incorporation into polymers or other materials can lead to advancements in areas such as electronics, coatings, or adhesives, where its aromatic and hydrophilic nature can enhance performance characteristics.

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

• 95950-06-4 1,2-bis-(2-chloro-phenyl)-1,2-diphenyl-ethane-1,2-diol 
• 108-38-3 m-xylene 
• 5162-03-8 (2-chlorophenyl)(phenyl)methanone 
• 615-41-8 2-iodochlorobenzene 
• 100-52-7 benzaldehyde 
• 934-56-5 trimethyl(phenyl)stannane 
• 89-98-5 2-chloro-benzaldehyde 
• 591-50-4 iodobenzene 
• 100-59-4 phenylmagnesium chloride 
• 949-38-2 1-(benzyloxy)-2-chlorobenzene 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 15842-76-9 (2-chloro-phenyl)-trimethyl-silane 
• 694-80-4 2-bromo-1-chlorobenzene 
• 591-51-5 phenyllithium 

Downstream Products

• 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 
• 56961-47-8 2-chloro-benzhydryl chloride 
• 1297593-92-0 1,3-diphenyl-3-(2-chlorophenyl)-1-propyne 
• 1509911-88-9 (E)-(3-(2-chlorophenyl)prop-1-ene-1,3-diyl)dibenzene 
• 2387-88-4 (2-{2-[(2-Chloro-phenyl)-phenyl-methoxy]-ethoxy}-ethyl)-dimethyl-amine 
• 29921-41-3 (o-benzyl)chlorobenzene 
• 16071-25-3 (S)-2-chlorobenzhydrol 

Relevant articles and documents

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Iodide as a Nucleophilic Trigger in Aryne Three-Component Coupling for the Synthesis of 2-Iodobenzyl Alcohols

The synthetic potential of KI as the iodide source in aryne three-component coupling has been demonstrated using aldehydes as the third component. This mild and transition-metal-free coupling reaction allowed the straightforward synthesis of 2-iodobenzyl alcohols in moderate to good yields with good functional group compatibility. Moreover, KBr and KCl could be used as the nucleophilic trigger in this aryne multicomponent coupling (MCC) and N-methylisatin and CO2 could be used as the electrophilic third components.

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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A Direct Br?nsted Acid-Catalyzed Azidation of Benzhydrols and Carbohydrates

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Employing Arynes for the Generation of Aryl Anion Equivalents and Subsequent Reaction with Aldehydes

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Synthetic method of diaryl methanol compound

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