1312765-94-8 Usage
Description
2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is a boronic acid derivative featuring a tetrahydroisoquinoline structure. It is utilized in organic synthesis and medicinal chemistry as a building block for the creation of diverse organic molecules. Known for its ability to form stable complexes with diols, this compound has found applications in the development of sensors, catalysts, and drugs. The presence of the tert-butoxycarbonyl group serves as a protective group in organic synthesis, enhancing the selectivity of chemical reactions. This makes 2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID a promising candidate for the development of pharmaceuticals and other organic compounds.
Uses
Used in Organic Synthesis:
2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is used as a building block for the synthesis of various organic molecules due to its versatile chemical structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is used as a key component in the development of pharmaceuticals, taking advantage of its ability to form stable complexes with biologically relevant molecules.
Used in Sensor Development:
2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is used as a component in the development of sensors, leveraging its capacity to form stable complexes with diols for detecting specific analytes.
Used in Catalyst Design:
2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is utilized in the design of catalysts, where its reactivity and complex-forming ability with diols contribute to enhancing the efficiency of chemical reactions.
Used in Drug Development:
In the pharmaceutical industry, 2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-6-YLBORONIC ACID is used as a potential drug candidate or a structural element in drug molecules, owing to its unique properties and the protective role of the tert-butoxycarbonyl group in enhancing the selectivity of chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 1312765-94-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,6 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1312765-94:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*6)+(3*5)+(2*9)+(1*4)=148
148 % 10 = 8
So 1312765-94-8 is a valid CAS Registry Number.
