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Di-n-butyl-(α-styrenyl)boronate is an organoboron compound with the chemical formula C12H21BO. It is a colorless liquid at room temperature and is soluble in organic solvents. di-n-butyl-(α-styrenyl)boronate is synthesized by the reaction of α-styrenylmagnesium bromide with di-n-butylboron bromide. Di-n-butyl-(α-styrenyl)boronate is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction. It is also employed in the synthesis of various organic compounds, such as polymers and pharmaceuticals, due to its ability to introduce the styrene moiety into target molecules. The compound is sensitive to air and moisture, and should be handled under an inert atmosphere.

1884-18-0

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1884-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1884-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1884-18:
(6*1)+(5*8)+(4*8)+(3*4)+(2*1)+(1*8)=100
100 % 10 = 0
So 1884-18-0 is a valid CAS Registry Number.

1884-18-0Relevant academic research and scientific papers

The preparation of optically active boronic ester substituted Δ2-isoxazolines

Wallace, Richard H.,Zong

, p. 87 - 91 (1999)

In this paper we report our recent results in the area of nitrile oxide cycloaddition to optically active vinylboronic esters to afford optically active boronic ester substituted Δ2-isoxazolines. In these studies, a number of optically active d

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