21945-66-4

Basic information

• Product Name: PHENYL-M-TOLYL-METHANOL
• Synonyms: PHENYL-M-TOLYL-METHANOL;AURORA KA-7056;(3-methylphenyl)-phenylmethanol
• CAS NO: 21945-66-4
• Molecular Formula: C₁₄H₁₄O
• Molecular Weight: 198.26
• Mol File: 21945-66-4.mol
• Article Data: 38

Chemical Properties

• Melting Point: 52 °C
• Boiling Point: 332.1°C at 760 mmHg
• Flash Point: 143.7°C
• Appearance: /
• Density: 1.081g/cm³
• Vapor Pressure: 5.94E-05mmHg at 25°C
• Refractive Index: 1.59
• PKA: 13.82±0.20(Predicted)
• CAS DataBase Reference: PHENYL-M-TOLYL-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYL-M-TOLYL-METHANOL(21945-66-4)
• EPA Substance Registry System: PHENYL-M-TOLYL-METHANOL(21945-66-4)

Safety Data

• Hazardous Substances Data: 21945-66-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H14O/c1-11-6-5-9-13(10-11)14(15)12-7-3-2-4-8-12/h2-10,14-15H,1H3

Upstream product

• 643-65-2 3-methyl benzophenone 
• 100-52-7 benzaldehyde 
• 28987-79-3 m-tolylmagnesium bromide 
• 120309-23-1 1,2-diphenyl-1,2-di-m-tolyl-ethane-1,2-diol 
• 103-73-1 Phenetole 
• 109-72-8 n-butyllithium 
• 100-58-3 phenylmagnesium bromide 
• 620-23-5 m-tolyl aldehyde 
• 52056-23-2 2-hydroxy-1,2-diphenyl-2-m-tolyl-ethanone 
• 10325-82-3 m-tolyllithium 
• 108-41-8 1-chloro-3-methylbenzene 
• 3262-89-3 triphenylboroxine 
• 79421-98-0 2,4,6-tris(m-tolyl)boroxine 
• 22071-15-4 ketoprofen 

Downstream Products

• 13391-36-1 3-methyl-benzhydryl chloride 
• 620-47-3 1-methyl-3-(phenylmethyl)-benzene 
• 51339-27-6 (3-methylphenyl)phenylbromomethane 
• 60423-38-3 2-(Phenyl-m-tolyl-methyl)-indan-1,3-dione 
• 7732-18-5 water 
• 643-65-2 3-methyl benzophenone 
• 167108-75-0 1-Methyl-4-(phenyl-m-tolyl-methoxy)-piperidine 
• 532984-25-1 (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid [1-phenyl-1-(3-tolyl)]-methyl ester 
• 1200120-11-1 1-phenyl-3-phenyl-3-(3-methylphenyl)-1-propyne 
• 1136166-73-8 phenyl(m-tolyl)methyl p-tolyl sulfone 
• 1426069-01-3 1,5-dimethyl-3-phenyl-3H-indene-2-carboxylic acid ethyl ester 
• 1426069-03-5 1,6-dimethyl-3-phenyl-3H-indene-2-carboxylic acid ethyl ester 
• 1426069-02-4 1,5-dimethyl-3-phenyl-3H-indene-2-carboxylic acid 
• 1426069-04-6 1,6-dimethyl-3-phenyl-3H-indene-2-carboxylic acid 

Relevant articles and documents

Experimental and density functional theory studies on hydroxymethylation of phenylboronic acids with paraformaldehyde over a Rh-PPh3 catalyst

The synthesis of benzyl alcohols (BAs) is highly vital for their wide applications in organic synthesis and pharmaceuticals. Herein, BAs was efficiently synthesized via hydroxymethylation of phenylboronic acids (PBAs) and paraformaldehyde over a simple Rh-PPh3 catalyst combined with an inorganic base (NaOH). A variety of BAs with the groups of CH3?, CH3O?, Cl?, Br?, and so on were obtained with moderate to good yields, indicating that the protocol had a good universality. Density functional theory (DFT) calculations proposed the Hayashi-type arylation mechanism involved the arylation step of PBA and Rh(OH)(PPh3)2 catalyst to form Rh(I)-bound aryl intermediates and the hydrolysis step of Rh(I)-bound aryl intermediates and HCHO to generate BA product (the rate-determining step). The present route provides a valuable and direct method for the synthesis of BAs and expands the application range of paraformaldehyde.

Synthesis and biological evaluation of new N-substituted 4-(arylmethoxy)piperidines as dopamine transporter inhibitors

The library of new N-substituted 4-(arylmethoxy)piperidines as dopamine transporter inhibitors was designed and synthesized. H-Bond donors in piperidine ring were found to be important for reduced locomotor activity in mice. 4-[Bis(4-fluorophenyl)methoxy]piperidine has IC50 17.0 ± 1.0 nm for dopamine transporter and locomotor activity, which is lower than that for cocaine.

Nickel Catalyzed Intermolecular Carbonyl Addition of Aryl Halide

In this study, we develop a nickel-catalyzed carbonyl arylation reaction employing aldehydes with aryl and allyl halides. Various aryl, α,β-unsaturated aldehyde and aliphatic aldehydes can be converted into their corresponding secondary alcohols in moderate-to-high yields. In addition, we extended this approach to develop an asymmetric reductive coupling reaction that combines nickel salts with chiral bisoxazoline ligands to give secondary alcohols with moderate enantioselectivity.