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benzene, [5-phenyl-3-(2-phenylethyl)pentyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66374-88-7

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66374-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66374-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,7 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 66374-88:
(7*6)+(6*6)+(5*3)+(4*7)+(3*4)+(2*8)+(1*8)=157
157 % 10 = 7
So 66374-88-7 is a valid CAS Registry Number.

66374-88-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(2-phenylethyl)methane

1.2 Other means of identification

Product number -
Other names 3-Phenaethyl-1,5-diphenyl-pentan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66374-88-7 SDS

66374-88-7Relevant academic research and scientific papers

A novel iron complex for cross-coupling reactions of multiple C-Cl bonds in polychlorinated solvents with grignard reagents

Gartia, Yashraj,Pulla, Sharon,Ramidi, Punnamchandar,Farris, Carolina Costa,Nima, Zeid,Jones, Darin E.,Biris, Alexandru S.,Ghosh, Anindya

, p. 1397 - 1404 (2013/01/15)

A novel iron(III) complex (2) of a pincer ligand [1, N2,N6-bis(2,6- diisopropylphenyl)pyridine-2,6-dicarboxamide] was developed and used for remediation of polychlorinated solvents via sp3-sp3 coupling of Grignard reagents with C-Cl bonds. The use of an iron catalyst for such coupling reactions is highly desirable due to its greener and more economical nature. Complex 2 was characterized using various spectroscopic techniques: electrospray ionization mass spectrometer (ESI-MS, m/z 575.1), cyclic voltammetry (E 1/2, 0.03 V and ΔE, 0.97 V), and ultraviolet visible (UV/Vis) spectroscopic techniques. The iron(III) complex showed efficient activation of multiple C-Cl bonds and catalyzing C-C coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents under ambient reaction conditions. Complex 2 showed exceptional activity with reactions approaching near completion in about 5 min. With the required catalyst loading as low as 0.2 mol%, considerably high turnover numbers (TON = 483) and turnover frequency (TOF = 5,800 h-1) were obtained. None of the products detected during the reaction contained any chlorine, indicating an efficient dechlorination method while synthesizing products of synthetic and commercial interest. Interestingly, the catalyst was capable of replacing all chlorine atoms in each polychlorinated solvent under the investigations with high conversion. Springer Science+Business Media, LLC 2012.

Cross coupling reactions of multiple CCl bonds of polychlorinated solvents with Grignard reagent using a pincer nickel complex

Gartia, Yashraj,Nasini, Udaya Bhasker,Ghosh, Anindya,Biswas, Abhijit,Stadler, Matthew

, p. 322 - 327,6 (2020/07/30)

The nickel(II) complex of a bulky pincer-type ligand, N,N′-bis(2,6- diisopropylphenyl)-2,6-pyridinedicarboxamido, was examined for sp 3-sp3 coupling of Grignard reagents with polychlorinated solvents. The nickel(II) complex catalyzed CC coupling of polychlorinated alkyl halides, such as dichloromethane (CH2Cl2), chloroform (CHCl3), and carbon tetrachloride (CCl4), with various Grignard reagents. The effective activation of multiple CCl bonds proceeded under ambient reaction conditions and within a short time (20 min). This catalyst displays the highest activity yet reported for this reaction type, with catalyst loading as low as 0.4 mol% and turnover frequency (TOF) as high as 724 h-1. The catalyst is capable of replacing all chlorine atoms with CC bond formations for all of the polychlorinated solvents under investigation. The catalytic process could prove to be an efficient method of remediation of toxic polychlorinated solvents while generating synthetically and commercially important chemicals.

Synthesis and Properties of the Tristyrylmethyl Anion

Komatsu, Koichi,Shirai, Shuzo,Tomioka, Isao,Okamoto, Kunio

, p. 1377 - 1380 (2007/10/02)

The title anion (3) having a C3v symmetric structure was generated from newly synthesized tristyrylmethane (4) and was characterized by means of 1H and 13C NMR spectroscopy.The pKa value of 4 was determined as 20.1 in DMSO-EtOH (9:1), indicatin

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