199609-62-6 Usage
Description
3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is a chemical compound featuring a phenylboronic acid core with a 3-((N-BOC-AMINO)METHYL) functional group. It serves as a versatile building block in organic synthesis and pharmaceutical research for the preparation of biologically active molecules. The N-BOC (tert-butyloxycarbonyl) group acts as a protecting agent for amino-containing compounds, allowing selective modifications, while the boronic acid group facilitates Suzuki-Miyaura coupling reactions for carbon-carbon bond formation. This makes 3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID a valuable intermediate for creating complex organic molecules across various applications.
Uses
Used in Organic Synthesis:
3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is used as a building block for the synthesis of complex organic molecules due to its ability to participate in various chemical reactions and form a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is used as a key intermediate for the development of biologically active molecules, leveraging its reactivity and the protective nature of the N-BOC group for selective modifications.
Used in Suzuki-Miyaura Coupling Reactions:
3-((N-BOC-AMINO)METHYL)PHENYLBORONIC ACID is utilized as a coupling partner in Suzuki-Miyaura reactions for the formation of carbon-carbon bonds, which is crucial for constructing molecular frameworks in organic chemistry and drug discovery.
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.
