1222533-84-7 Usage
Description
5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is a complex chemical compound characterized by a pyrrolopyridine ring system, which is a fusion of a pyrrole and a pyridine ring. 5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is notable for its incorporation of a fluorine atom and a unique boron-containing dioxaborolane group. The dioxaborolane group features a boron atom coordinated to two oxygen atoms and a tetramethyl group, which contributes to the compound's reactivity and potential applications in chemical synthesis.
Uses
Used in Medicinal Chemistry:
5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is utilized as a building block in medicinal chemistry for the synthesis of pharmaceuticals and other bioactive compounds. Its unique structure and the presence of a fluorine atom, which can influence the compound's lipophilicity and metabolic stability, make it a valuable component in the development of new drugs.
Used in Drug Development:
In the field of drug development, 5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is employed as a precursor for the creation of novel chemical entities. Its biological activity and the versatility of the boron atom for various chemical reactions allow for the exploration of its potential in the synthesis of new therapeutic agents.
Used in Chemical Synthesis:
5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is used as a versatile intermediate in chemical synthesis. The boron atom in the dioxaborolane group can participate in a range of reactions, such as Suzuki-Miyaura cross-coupling, which is a widely used method for the formation of carbon-carbon bonds. This makes the compound a valuable tool for the synthesis of complex organic molecules and the modification of existing compounds to enhance their properties or introduce new functionalities.
Used in Bioactive Compounds Synthesis:
5-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine is also used in the synthesis of bioactive compounds, where its unique structure can contribute to the development of molecules with specific biological activities. The presence of the pyrrolopyridine ring system and the fluorine atom can influence the compound's interaction with biological targets, potentially leading to the discovery of new therapeutic agents or probes for biological research.
Check Digit Verification of cas no
The CAS Registry Mumber 1222533-84-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,2,5,3 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1222533-84:
(9*1)+(8*2)+(7*2)+(6*2)+(5*5)+(4*3)+(3*3)+(2*8)+(1*4)=117
117 % 10 = 7
So 1222533-84-7 is a valid CAS Registry Number.
1222533-84-7Relevant articles and documents
IMPROVED PROCESS FOR PREPARING BORYL 7-AZAINDOLE COMPOUNDS
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Page/Page column 23, (2016/12/22)
The present disclosure relates to an improved process for the preparation of 3-boryl substituted azaindole compounds in high yields and high selectivity. Such azaindole compounds may be used as intermediates to form compounds with cytotoxic, anticancer, and antiviral activities.
