6266-56-4

Basic information

• Product Name: bis(4-methylphenyl)(phenyl)methanol
• Synonyms: bis(4-methylphenyl)(phenyl)methanol
• CAS NO: 6266-56-4
• Molecular Formula: C₂₁H₂₀O
• Molecular Weight: 288.3829
• Mol File: 6266-56-4.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 444.5°Cat760mmHg
• Flash Point: 172.2°C
• Appearance: /
• Density: 1.097g/cm³
• Vapor Pressure: 1.11E-08mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: bis(4-methylphenyl)(phenyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: bis(4-methylphenyl)(phenyl)methanol(6266-56-4)
• EPA Substance Registry System: bis(4-methylphenyl)(phenyl)methanol(6266-56-4)

Safety Data

• Hazardous Substances Data: 6266-56-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C21H20O/c1-16-8-12-19(13-9-16)21(22,18-6-4-3-5-7-18)20-14-10-17(2)11-15-20/h3-15,22H,1-2H3

Upstream product

• 108-86-1 bromobenzene 
• 611-97-2 bis(p-methylphenyl)-methanone 
• 611-73-4 Benzoylformic acid 
• 93-58-3 benzoic acid methyl ester 
• 4294-57-9 para-methylphenylmagnesium bromide 
• 93-89-0 benzoic acid ethyl ester 
• 583-04-0 vinyl benzoate 
• 13948-06-6 bis(4-methylphenyl)phenylmethylium 
• 98-88-4 benzoyl chloride 
• 106-38-7 para-bromotoluene 
• 1137-11-7 1-benzoyl-3,5-dimethyl-1H-pyrazole 
• 591-51-5 phenyllithium 
• 1254223-74-9 Me₂Tr-OAc 
• 134-84-9 4-Methylbenzophenone 

Downstream Products

• 69239-35-6 Chlorbis(4-methylphenyl)phenylmethan 
• 95431-25-7 3-Phenyl-3,3-bis-(4-methyl-phenyl)-propionsaeure 
• 94863-94-2 3,6-Dimethyl-9-phenyl-fluoren 
• 35960-00-0 α-(p-Carboxyphenyl)-α-hydroxy-α-phenyl-p-toluic Acid 
• 82313-76-6 4,4'-Bis(brommethyl)triphenylmethanol 
• 13948-06-6 bis(4-methylphenyl)phenylmethylium 
• 82313-74-4 4,4'-Bis(brommethyl)triphenylmethan 
• 102599-21-3 phenyl-di-p-tolyl-acetic acid 
• 112214-31-0 methyl-2,3-di-O-acetyl-4-O-(di-p-tolyl)phenylmethyl-β-D-xylopyranoside 
• 82313-72-2 15-Hydroxy-15-phenyl-2,7-dithia<1.8>paracyclophan 
• 82313-73-3 15-Hydroxy-15-phenyl-2,7-dithia<1.8>paracyclophan-2,2,7,7-tetraoxid 
• 82272-68-2 13-Hydroxy-13-phenyl<1.6>paracyclophan 
• 603-39-4 4,4′-(phenylmethylene)bis(methylbenzene) 
• 35960-02-2 Bis-(p-hydroxymethylphenyl)-phenylmethanol 

Relevant articles and documents

Kinetically Controlled, Highly Chemoselective Acylation of Functionalized Grignard Reagents with Amides by N?C Cleavage

The direct transition-metal-free acylation of amides with functionalized Grignard reagents by highly chemoselective N?C cleavage under kinetic control has been accomplished. The method offers rapid and convergent access to functionalized biaryl ketones through transient tetrahedral intermediates. The direct access to functionalized Grignard reagents by in situ halogen–magnesium exchange promoted by the versatile turbo-Grignard reagent (iPrMgCl?LiCl) permits excellent substrate scope with respect to both the amide and Grignard coupling partners. These reactions enable facile, operationally simple and chemoselective access to tetrahedral intermediates from amides under significantly milder conditions than chelation-controlled intermediates. This novel direct two-component coupling sets the stage for using amides as acylating reagents in an alternative paradigm to the metal-chelated approach, acyl metals and Weinreb amides.

Optimized S-trityl-l-cysteine-based inhibitors of kinesin spindle protein with potent in vivo antitumor activity in lung cancer xenograft models

The mitotic kinesin Eg5 is critical for the assembly of the mitotic spindle and is a promising chemotherapy target. Previously, we identified S-trityl-l-cysteine as a selective inhibitor of Eg5 and developed triphenylbutanamine analogues with improved pot

Synthesis and electron transfer characteristics of a neutral, low-band-gap, mixed-valence polyradical

A polyradical consisting of alternating triarylamine and perchlorotriphenylmethyl radical moieties was synthesized by Horner-Emmons reaction. This compound is the first polymeric neutral mixed-valence compound that shows an intervalence charge transfer (I