296768-49-5 Usage
General Description
5-(4-Methylphenyl)Thiophene-2-boronic acid is a chemical compound with the molecular formula C12H13BO2S. It is a boronic acid derivative with a thiophene ring and a methylphenyl group attached to it. Boronic acids are known for their ability to form reversible covalent bonds with cis-diols, making them useful in various chemical reactions and biological applications. This specific compound has potential applications in organic synthesis, pharmaceutical research, and materials science due to its unique structure and reactivity. It may also be used as a building block for the synthesis of more complex organic compounds and as a ligand in catalytic processes.
Check Digit Verification of cas no
The CAS Registry Mumber 296768-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 296768-49:
(8*2)+(7*9)+(6*6)+(5*7)+(4*6)+(3*8)+(2*4)+(1*9)=215
215 % 10 = 5
So 296768-49-5 is a valid CAS Registry Number.
296768-49-5Relevant articles and documents
SYSTEM FOR CONTROLLING THE REACTIVITY OF BORONIC ACIDS
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Page/Page column 15, (2009/02/11)
A protected organoboronic acid includes a boron having an sp3 hybridization, a conformationally rigid protecting group bonded to the boron, and an organic group bonded to the boron through a boron-carbon bond. A method of performing a chemical reaction includes contacting a protected organoboronic acid with a reagent, the protected organoboronic acid including a boron having an sp3 hybridization, a conformationally rigid protecting group bonded to the boron, and an organic group bonded to the boron through a boron-carbon bond. The organic group is chemically transformed, and the boron is not chemically transformed.
