669713-95-5 Usage
Uses
Used in Pharmaceutical Synthesis:
4-N-Boc-amino-3-methoxyphenylboronic acid is used as a key building block for the synthesis of various pharmaceuticals and bioactive molecules. Its unique structure allows for the creation of diverse chemical entities with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, 4-N-Boc-amino-3-methoxyphenylboronic acid is utilized as a reagent for Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in the construction of complex organic molecules.
Used in Medicinal Chemistry:
4-N-Boc-amino-3-methoxyphenylboronic acid is employed as a valuable intermediate in the development of new drugs, taking advantage of its boronic acid functionality and Boc protecting group to create molecules with specific biological activities.
Used in Chemical Synthesis for Selective Modification:
The presence of the Boc protecting group in 4-N-Boc-amino-3-methoxyphenylboronic acid allows for selective modification of the amino group, which is crucial in the synthesis of complex molecules with specific functional groups and properties. This selective modification expands its utility in the preparation of targeted chemical compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 669713-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,7,1 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 669713-95:
(8*6)+(7*6)+(6*9)+(5*7)+(4*1)+(3*3)+(2*9)+(1*5)=215
215 % 10 = 5
So 669713-95-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H18BNO5/c1-12(2,3)19-11(15)14-9-6-5-8(13(16)17)7-10(9)18-4/h5-7,16-17H,1-4H3,(H,14,15)
