762262-11-3 Usage
Uses
Used in Organic Synthesis:
3-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID is used as a reagent for forming carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its boronic acid functional group allows for selective binding to biomolecules, making it a valuable component in the synthesis of complex organic compounds.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 3-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID is used as a building block for the development of biologically active compounds. Its ability to selectively bind to biomolecules and its potential for chemical derivatization make it a promising candidate for the creation of new pharmaceuticals.
Used in Drug Development:
3-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID is employed as a key component in the development of drugs targeting specific biomolecules. Its selective binding properties and versatility in chemical modification contribute to the design and synthesis of novel therapeutic agents with improved efficacy and selectivity.
Used in Chemical Derivatization:
In the field of chemical research, 3-(2-CYANOETHYLAMINOCARBONYL)PHENYLBORONIC ACID is used as a versatile building block for the synthesis of various chemical derivatives. Its cyanoethylaminocarbonyl group provides opportunities for further chemical modification, enabling the development of new compounds with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 762262-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,2,2,6 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 762262-11:
(8*7)+(7*6)+(6*2)+(5*2)+(4*6)+(3*2)+(2*1)+(1*1)=153
153 % 10 = 3
So 762262-11-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BN2O3/c12-5-2-6-13-10(14)8-3-1-4-9(7-8)11(15)16/h1,3-4,7,15-16H,2,6H2,(H,13,14)
