669713-95-5 Usage
General Description
4-N-Boc-amino-3-methoxyphenylboronic acid is a chemical compound with the molecular formula C13H19BNO5. It is a boronic acid derivative that contains both an amino group and a Boc (tert-butoxycarbonyl) protecting group. 4-N-Boc-amino-3-methoxyphenylboronic acid is often used in organic and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and bioactive molecules. Its boronic acid functionality makes it a valuable reagent for Suzuki-Miyaura coupling reactions, which are commonly used in medicinal chemistry to form carbon-carbon bonds. Additionally, the presence of the Boc protecting group allows for selective modification of the amino group, further expanding its utility in chemical synthesis.
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)