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40982-58-9

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40982-58-9 Usage

Description

2,4-Bis[(triMethylsilyl)oxy]pyridine is an organic compound characterized by its unique structure, which features a pyridine ring with two triMethylsilyl groups attached to the 2nd and 4th positions via oxygen atoms. 2,4-Bis[(triMethylsilyl)oxy]pyridine is known for its potential applications in the synthesis of various pharmaceutical compounds.

Uses

Used in Pharmaceutical Industry:
2,4-Bis[(triMethylsilyl)oxy]pyridine is used as an intermediate in the synthesis of 3-Deazapyrimidine, which is a key component in the development of neoplasm inhibitors. These inhibitors are essential in the treatment of various types of cancer, as they target and inhibit the growth of tumor cells.
In the synthesis of 3-Deazapyrimidine, 2,4-Bis[(triMethylsilyl)oxy]pyridine serves as a crucial building block, providing the necessary structural framework for the formation of the final product. 2,4-Bis[(triMethylsilyl)oxy]pyridine's unique properties, such as its reactivity and stability, make it an ideal candidate for use in the development of novel cancer-fighting drugs.
Furthermore, the versatility of 2,4-Bis[(triMethylsilyl)oxy]pyridine allows it to be employed in the synthesis of other bioactive molecules with potential applications in the pharmaceutical industry. Its ability to form various derivatives and analogs enables researchers to explore a wide range of chemical modifications, potentially leading to the discovery of new and more effective therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 40982-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,8 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40982-58:
(7*4)+(6*0)+(5*9)+(4*8)+(3*2)+(2*5)+(1*8)=129
129 % 10 = 9
So 40982-58-9 is a valid CAS Registry Number.

40982-58-9Downstream Products

40982-58-9Relevant articles and documents

Synthesis and biological evaluation of 3,3-difluoropyridine-2,4(1H,3H)- dione and 3-deaza-3-fluorouracil base and nucleoside derivatives

Robins, Morris J.,Yang, Hong,Miranda, Karl,Peterson, Matt A.,De Clercq, Erik,Balzarini, Jan

experimental part, p. 3018 - 3027 (2010/02/28)

New 3-deaza-3-halouracil nucleosides including 3-deaza-3-fluorouridine and its 2′-deoxy and arabino analogues have been prepared by fluorination of protected precursors. The resulting 3,3-difluoropyridine-2,4(1H,3H)-dione derivatives underwent palladium-c

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