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1628317-93-0

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  • N-(Piperidin-4-yl)-6-(2,2,2-trifluoroethyl)thieno[2,3-d]pyrimidin-4-amine

    Cas No: 1628317-93-0

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1628317-93-0 Usage

General Description

N-(Piperidin-4-Yl)-6-(2,2,2-Trifluoroethyl)Thieno[2,3-D]Pyrimidin-4-Amine is a chemical compound that belongs to the thieno[2,3-d]pyrimidine class. It consists of a piperidine ring attached to a thieno[2,3-d]pyrimidine moiety, with a 2,2,2-trifluoroethyl group attached to position 6 of the thieno[2,3-d]pyrimidine ring. N-(Piperidin-4-Yl)-6-(2,2,2-Trifluoroethyl)Thieno[2,3-D]Pyrimidin-4-Amine may have potential pharmacological applications due to its unique structure, and it could be used as a starting point for the development of new drugs targeting specific biological pathways or receptors. Additionally, it may also have uses in the field of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1628317-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,8,3,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1628317-93:
(9*1)+(8*6)+(7*2)+(6*8)+(5*3)+(4*1)+(3*7)+(2*9)+(1*3)=180
180 % 10 = 0
So 1628317-93-0 is a valid CAS Registry Number.

1628317-93-0Downstream Products

1628317-93-0Relevant articles and documents

METHODS OF PROMOTING BETA CELL PROLIFERATION

-

, (2018/06/30)

The present disclosure provides methods of promoting proliferation of a pancreatic cell. The methods are useful for the treatment of diabetes and other diseases characterized by impaired glucose tolerance.

Design and synthesis of benzylpiperidine inhibitors targeting the menin–MLL1 interface

Ren, Jing,Xu, Wei,Tang, Le,Su, Minbo,Chen, Danqi,Chen, Yue-Lei,Zang, Yi,Li, Jia,Shen, Jingkang,Zhou, Yubo,Xiong, Bing

supporting information, p. 4472 - 4476 (2016/08/25)

Menin is an essential oncogenic cofactor for mixed lineage leukemia (MLL)-mediated leukemogenesis, functioning through its direct interaction with MLL1 protein. Therefore, targeting the menin–MLL1 protein–protein interface represents a promising strategy

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