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Borane, difluoro(4-methylphenyl)-, also known as 4-methylphenylborane difluoride, is an organoborane compound with the chemical formula C7H8BF2. It is a colorless, volatile, and moisture-sensitive liquid that is widely used in organic synthesis as a reducing agent and a Lewis acid. borane, difluoro(4-methylphenyl)- is formed by the reaction of 4-methylphenylmagnesium bromide with boron trifluoride, resulting in the formation of a stable complex. Borane, difluoro(4-methylphenyl)-, is known for its ability to selectively reduce aldehydes, ketones, and esters, making it a valuable reagent in the synthesis of various organic compounds. Due to its sensitivity to moisture and air, it is typically stored under an inert atmosphere and used in a controlled environment.

768-39-8

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768-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 768-39-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 768-39:
(5*7)+(4*6)+(3*8)+(2*3)+(1*9)=98
98 % 10 = 8
So 768-39-8 is a valid CAS Registry Number.

768-39-8Downstream Products

768-39-8Relevant academic research and scientific papers

On-off QD switch that memorizes past recovery from quenching by diazonium salts

Liras, Marta,Gonzalez-Bejar, Maria,Scaiano

experimental part, p. 9757 - 9762 (2011/04/25)

The understanding of the interaction of CdSe/ZnS semiconductor quantum dots (QD) with their chemical environment is fundamental, yet far from being fully understood. p-Methylphenyldiazonium tetrafluoroborate has been used to get some insight into the effect of diazonium salts on the spectroscopy of QD. Our study reveals that the surface of CdSe/ZnS quantum dots can be modified by diazonium salts (although not functionalized), showing and on-off fluorescence behaviour that memorizes past quenching recoveries. Facile modification of the surface confers protection against quenching by new molecules of diazonium salt and other known quenchers such as 4-amino-TEMPO. The reaction mechanism has been explored in detail by using different spectroscopic techniques. At the first time after addition of diazonium salt over QD the fluorescent is turned off with Stern-Volmer behaviour; the fluorescence recovers following irradiation. Subsequent additions of diazonium salts do not cause the same degree of quenching. We have noted that the third addition (following two cycles of addition and irradiation) is unable to quench the fluorescence. Monitoring the process using NMR techniques reveals the formation of p-difluoroborane toluene as a result of the irradiation of diazonium-treated QD; the treatment leads to the fluorination of the QD surface.

A New Borylation Method for Alkylbenzene and Polystyrene

Paetzold, Peter,Hoffmann, Juergen

, p. 3724 - 3733 (2007/10/02)

The borylation of alkylbenzenes by Hal2BH (Hal = F, Cl, Br) gives H2 and a mixture of m- and p-alkyl(dihaloboryl)benzenes.In the case of bulky alkyl groups, such as isopropyl, tert-butyl, these are partially split off as R - H and RBHal2.The phenyl groups in polystyrene-divinylbenzene copolymers undergo borylation with Br2BH in a 55percent yield.

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