942069-53-6 Usage
Class
The compound belongs to the class of dioxaborolane compounds.
Structure
It has a unique structure with a bromine atom attached to a methylphenyl group and four methyl groups attached to the boron atom.
Usage
It is commonly used as a reagent in organic synthesis, particularly in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds.
Stability
It is known for its stability and compatibility with a wide range of functional groups, making it a versatile tool in organic chemistry.
Importance
Its unique structure and properties make it an important building block for the synthesis of pharmaceuticals, agrochemicals, and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 942069-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,0,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 942069-53:
(8*9)+(7*4)+(6*2)+(5*0)+(4*6)+(3*9)+(2*5)+(1*3)=176
176 % 10 = 6
So 942069-53-6 is a valid CAS Registry Number.
942069-53-6Relevant articles and documents
INTERMOLECULAR C-H SILYLATION OF UNACTIVATED ARENES
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Paragraph 00117; 00124, (2015/03/28)
Reaction mixtures for silvlating arene substrates and methods of using such reaction mixtures to silyiate the arene substrates are provided. Exemplary reaction mixtures include the arene substrate, a liganded metal catalyst, a hydrogen acceptor and an organic solvent. The reaction conditions allow for diverse substituents on the arene substrate.
