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64634-52-2

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64634-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64634-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,3 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64634-52:
(7*6)+(6*4)+(5*6)+(4*3)+(3*4)+(2*5)+(1*2)=132
132 % 10 = 2
So 64634-52-2 is a valid CAS Registry Number.

64634-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[bis(4-fluorophenyl)methyl]-4-fluorobenzene

1.2 Other means of identification

Product number -
Other names -

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:64634-52-2 SDS

64634-52-2Downstream Products

64634-52-2Relevant articles and documents

Transition-Metal-Free Synthesis of Polyfunctional Triarylmethanes and 1,1-Diarylalkanes by Sequential Cross-Coupling of Benzal Diacetates with Organozinc Reagents

Wei, Baosheng,Ren, Qianyi,Bein, Thomas,Knochel, Paul

, p. 10409 - 10414 (2021/03/26)

A variety of functionalized triarylmethane and 1,1-diarylalkane derivatives were prepared via a transition-metal-free, one-pot and two-step procedure, involving the reaction of various benzal diacetates with organozinc reagents. A sequential cross-coupling is enabled by changing the solvent from THF to toluene, and a two-step SN1-type mechanism was proposed and evidenced by experimental studies. The synthetic utility of the method is further demonstrated by the synthesis of several biologically relevant molecules, such as an anti-tuberculosis agent, an anti-breast cancer agent, a precursor of a sphingosine-1-phosphate (S1P) receptor modulator, and a FLAP inhibitor.

The Reduction of Fluorine-containing Triarylmethanols by Formic Acid

Andrews, Adrian F.,Mackie, Raymond K.,Walton, John C.

, p. 96 - 102 (2007/10/02)

Triarylmethanols containing one or more fluorine substituents in the para-positions are converted by 90 percent formic acid into a mixture of the fluorine-containing triarylmethane, and a second component in which one fluorine has been replaced by a hydro

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