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1-fluoro-4-(phenyl(p-tolyl)methyl)benzene is an organic compound characterized by a benzene ring with a fluorine atom at the 1st position, and a phenyl(p-tolyl)methyl group attached at the 4th position. This molecule consists of a benzene ring with a fluorine atom, a phenyl group, and a p-tolyl group (a methyl group attached to a phenyl ring) bonded to a methylene bridge. The compound has a molecular formula of C19H17F, and its structure can be represented as C6H5-F-C6H4-CH(C6H5)-CH3. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties.

39768-77-9

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39768-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39768-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,6 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39768-77:
(7*3)+(6*9)+(5*7)+(4*6)+(3*8)+(2*7)+(1*7)=179
179 % 10 = 9
So 39768-77-9 is a valid CAS Registry Number.

39768-77-9Downstream Products

39768-77-9Relevant academic research and scientific papers

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)

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.

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