199609-62-6 Usage
General Description
3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is a chemical compound that consists of a phenylboronic acid core with a 3-((N-BOC-AMINO)METHYL) functional group attached. 3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is often used in organic synthesis and pharmaceutical research as a versatile building block for the preparation of various biologically active molecules. The N-BOC (tert-butyloxycarbonyl) group is a protecting group that can be removed under mild conditions, making it useful for the selective modification of amino-containing compounds. Additionally, the boronic acid group makes this compound suitable for use in Suzuki-Miyaura coupling reactions for the formation of carbon-carbon bonds. Overall, 3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is a valuable intermediate in the preparation of complex organic molecules for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 199609-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 199609-62:
(8*1)+(7*9)+(6*9)+(5*6)+(4*0)+(3*9)+(2*6)+(1*2)=196
196 % 10 = 6
So 199609-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H18BNO4/c1-12(2,3)18-11(15)14-8-9-5-4-6-10(7-9)13(16)17/h4-7,16-17H,8H2,1-3H3,(H,14,15)
199609-62-6Relevant articles and documents
Small molecule thienopyrimidine-based protein tyrosine kinase inhibitors
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Page/Page column 40, (2010/02/15)
Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.
