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(4-ethylphenyl)dichloroborane is an organoborane compound with the chemical formula C8H10BCl2. It is a colorless liquid at room temperature and is derived from the substitution of two hydrogen atoms in boron trichloride (BCl3) with a 4-ethylphenyl group. (4-ethylphenyl)dichloroborane is an important reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the hydroboration reaction. It is also used as a Lewis acid catalyst in various chemical transformations. Due to its reactivity, (4-ethylphenyl)dichloroborane should be handled with care, as it can be sensitive to moisture and air.

4250-50-4

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4250-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4250-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4250-50:
(6*4)+(5*2)+(4*5)+(3*0)+(2*5)+(1*0)=64
64 % 10 = 4
So 4250-50-4 is a valid CAS Registry Number.

4250-50-4Downstream Products

4250-50-4Relevant academic research and scientific papers

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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