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2-Bromothieno[2,3-c]pyridin-7(6H)-one is a heterocyclic compound characterized by the presence of a thieno[2,3-c]pyridine core, which is a fused ring system consisting of a thiophene and a pyridine. The compound features a bromine atom at the 2-position and a ketone functional group at the 7-position, which is part of a 6-membered ring (6H). This chemical structure is significant in organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other organic compounds due to its unique electronic and steric properties. The compound's specific reactivity, stability, and potential uses would depend on its physical and chemical properties, which are influenced by the presence of the bromine substituent and the ketone group.

960289-04-7

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960289-04-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960289-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,2,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 960289-04:
(8*9)+(7*6)+(6*0)+(5*2)+(4*8)+(3*9)+(2*0)+(1*4)=187
187 % 10 = 7
So 960289-04-7 is a valid CAS Registry Number.

960289-04-7Relevant academic research and scientific papers

METHODS AND COMPOSITIONS FOR MODULATING SPLICING

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, (2020/08/22)

Described herein are small molecule splicing modulator compounds that modulate splicing of mRNA, such as pre-mRNA, encoded by genes, and methods of use of the small molecule splicing modulator compounds for modulating splicing and treating diseases and conditions.

IN-FLOW PHOTOOXYGENATION OF AMINOTHIENOPYRIDINONES GENERATES NOVEL PTP4A3 PHOSPHATASE INHIBITORS

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Paragraph 00166, (2020/06/05)

The disclosure provides compounds that inhibit protein tyrosine phosphatase, such as protein tyrosine phosphatase 4A3 (PTP4A3). The disclosure also provides pharmaceutical compositions, uses, and methods of using the compounds, such as in the treatment of cancers. (I), wherein X is O or NH.

In-flow photooxygenation of aminothienopyridinones generates iminopyridinedione PTP4A3 phosphatase inhibitors

Tasker, Nikhil R.,Rastelli, Ettore J.,Blanco, Isabella K.,Burnett, James C.,Sharlow, Elizabeth R.,Lazo, John S.,Wipf, Peter

, p. 2448 - 2466 (2019/03/06)

A continuous flow photooxygenation of 7-aminothieno[3,2-c]pyridin-4(5H)-ones to produce 7-iminothieno[3,2-c]pyridine-4,6(5H,7H)-diones has been developed, utilizing ambient air as the sole reactant. N-H Imines are formed as the major products, and excellent functional group tolerance and conversion on gram-scale without the need for chromatographic purification allow for facile late-stage diversification of the aminothienopyridinone scaffold. Several analogs exhibit potent in vitro inhibition of the cancer-associated protein tyrosine phosphatase PTP4A3, and the SAR supports an exploratory docking model.

NOVEL MCH RECEPTOR ANTAGONISTS

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, (2008/06/13)

The present invention relates to a melanin concentrating hormone antagonist compound of formula (I): wherein R1, Ra, Rb, R2, L1, R3, R4 and R5 are as defined, or a pharmaceutically acceptable salt, enantiomer, diastereomer or mixture of diasteromers thereof useful in the treatment, obesity and related diseases.

NOVEL MCH RECEPTOR ANTAGONISTS

-

, (2008/06/13)

The present invention relates to a melanin concentrating hormone antagonist compound of formula (I): wherein R1, Ra, Rb, R2, L1, R3, R4 and R5 are as defined, or a pharmaceutically acceptable salt, enantiomer, diastereomer or mixture of diasteromers thereof useful in the treatment, obesity and related diseases.

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