77509-50-3 Usage
Chemical Class
2-(4-bromophenyl)-2,3-dihydro-1H-1,3,2-benzodiazaborole belongs to the class of benzodiazaborole derivatives.
Molecular Structure
It contains a benzene ring with a bromine atom attached to the 4th position and a boron atom attached to the 2nd position of the benzene ring.
Medicinal Chemistry Applications
It serves as a versatile building block for the synthesis of various biologically active molecules.
Anti-bacterial and Anti-fungal Properties
It is being investigated for its potential as an anti-bacterial and anti-fungal agent.
New Material and Pharmaceutical Development
It has shown promise in the development of new materials and pharmaceuticals.
Need for Further Research
Further research and exploration of its properties are warranted to fully understand its potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 77509-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,0 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77509-50:
(7*7)+(6*7)+(5*5)+(4*0)+(3*9)+(2*5)+(1*0)=153
153 % 10 = 3
So 77509-50-3 is a valid CAS Registry Number.
77509-50-3Relevant academic research and scientific papers
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.
