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2-(2-methoxyphenyl)-1,3-dihydro-1H-benzo[d]1,3,2-diazaborole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1643375-82-9

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1643375-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1643375-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,3,3,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1643375-82:
(9*1)+(8*6)+(7*4)+(6*3)+(5*3)+(4*7)+(3*5)+(2*8)+(1*2)=179
179 % 10 = 9
So 1643375-82-9 is a valid CAS Registry Number.

1643375-82-9Relevant academic research and scientific papers

Palladium-catalysed cross-coupling reaction of ultra-stabilised 2-aryl-1,3-dihydro-1H-benzo[d]1,3,2-diazaborole compounds with aryl bromides: A direct protocol for the preparation of unsymmetrical biaryls

Sithebe, Siphamandla,Robinson, Ross S.

, p. 1107 - 1113 (2014)

There has been a significant interest in organoboron compounds such as arylboronic acids, arylboronate esters and potassium aryltrifluoroborate salts because they are versatile coupling partners in metal-catalysed cross-coupling reactions. On the other hand, their nitrogen analogues, namely, 1,3,2-benzodiazaborole-type compounds have been studied extensively for their intriguing absorption and fluorescence characteristics. Here we describe the first palladium-catalysed Suzuki-Miyaura cross-coupling reaction of easily accessible and ultra-stabilised 2-aryl-1,3-dihydro-1H-benzo[d]1,3,2-diazaborole derivatives with various aryl bromides. Aryl bromides bearing electron-withdrawing, electron-neutral and electron-donating substituents are reacted under the catalytic system furnishing unsymmetrical biaryl products in isolated yields of up to 96% in only 10 minutes.

Synthesis of Functionalized 1,3,2-Benzodiazaborole Cores Using Bench-Stable Components

Davies, Geraint H. M.,Molander, Gary A.

, p. 3771 - 3779 (2016/05/24)

The azaborine motif provides a unique opportunity to develop core isosteres by inserting B-N units in place of C-C bonds within aromatic scaffolds, creating new pseudoaromatic building blocks that retain comparable structural features. Previous synthetic routes to the 1,3,2-benzodiazaborole core have used organoboron dichlorides and boronic acids as the boron precursors. The transformation developed herein utilizes entirely bench stable starting materials, including organotrifluoroborates, enabling a wider array of substrate analogues under facile reaction conditions. Furthermore, physical, structural, and electronic properties of these compounds were explored computationally to understand the influence of the B-N replacement on the structure, aromaticity, and isosteric viability of these analogues.

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