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1H-Pyrrolo[2,3-b]pyridine, 4,5-difluoro-1-[tris(1-methylethyl)silyl]is a chemical compound that belongs to the class of pyrrolopyridines. It features a pyrrolopyridine core with two fluorine atoms and a tris(1-methylethyl)silyl group attached at specific positions. This unique structure and properties make it a valuable building block in the development of novel compounds and materials for various industrial and research purposes.

685513-89-7

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685513-89-7 Usage

Uses

Used in Organic Synthesis:
1H-Pyrrolo[2,3-b]pyridine, 4,5-difluoro-1-[tris(1-methylethyl)silyl]is used as a key intermediate in organic synthesis for the creation of complex organic molecules. Its fluorine atoms and tris(1-methylethyl)silyl group facilitate various chemical reactions, making it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1H-Pyrrolo[2,3-b]pyridine, 4,5-difluoro-1-[tris(1-methylethyl)silyl]is used as a starting material for the development of new drugs. Its unique structure allows for the design of molecules with specific biological activities, targeting a range of therapeutic areas such as oncology, neurology, and infectious diseases.
Used in Materials Science:
1H-Pyrrolo[2,3-b]pyridine, 4,5-difluoro-1-[tris(1-methylethyl)silyl]is also utilized in materials science for the development of advanced materials with tailored properties. Its incorporation into polymers, coatings, and other materials can enhance their performance, making them suitable for applications in electronics, aerospace, and other high-tech industries.

Check Digit Verification of cas no

The CAS Registry Mumber 685513-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,5,1 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 685513-89:
(8*6)+(7*8)+(6*5)+(5*5)+(4*1)+(3*3)+(2*8)+(1*9)=197
197 % 10 = 7
So 685513-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H24F2N2Si/c1-10(2)21(11(3)4,12(5)6)20-8-7-13-15(18)14(17)9-19-16(13)20/h7-12H,1-6H3

685513-89-7Downstream Products

685513-89-7Relevant academic research and scientific papers

Compound serving as protein kinase inhibitor and application of compound

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Paragraph 0359-0360; 0365-0366, (2021/04/07)

The invention discloses a compound used as a protein kinase inhibitor and application of the compound, the compound has an obvious inhibition effect on protein kinase activity, can be used as a BTK inhibitor for preparing medicines for treating BTK-mediated diseases such as malignant tumors, autoimmune diseases and the like, and has wide application prospect.

AZAINDOLE CARBOXAMIDE COMPOUNDS FOR THE TREATMENT OF MYCOBACTERIAL INFECTIONS

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Page/Page column 104, (2021/04/02)

Provided herein are compounds of Formula (I) and Formula (II): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of tuberculosis.

OXADIAZINE COMPOUNDS AND METHODS OF USE THEREOF

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Paragraph 0595, (2017/03/14)

The present disclosure relates to oxadiazine compounds, pharmaceutical compositions comprising an effective amount of an oxadiazine compound and methods for using an oxadiazine compound in the treatment of a neurodegenerative disease, comprising administering to a subject in need thereof an effective amount of an oxadiazine compound.

1H-PYRROLO[2,3-B] PYRIDINE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS

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Page/Page column 30; 81; 82, (2013/08/15)

The inventions relates to compounds of (I) and therapeutic uses thereof : (I) The terms Z, Y, and R1 are as defined in the claims.

PYRROLOPYRIDINES AS KINASE INHIBITORS

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Page/Page column 100-101, (2009/12/23)

Compounds of Formula (I) are useful for inhibition of CHKl and/or CHK2. Methods of using compounds of Formula (I) and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.

Synthesis of functionalized 7-azaindoles via directed ortho-metalations

L'Heureux, Alexandre,Thibault, Carl,Ruel, Réjean

, p. 2317 - 2319 (2007/10/03)

Functionalization at C-5 of 4-fluoro- and 4-chloro-1-triisopropylsilyl-7- azaindole, 1 and 2, respectively, leads to a variety of new substituted 7-azaindole derivatives. We also describe two approaches to introduce functionality at C-6.

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