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5,7-DICHLORO-1H-[1,6]NAPHTHYRIDIN-4-ONE is a heterocyclic chemical compound belonging to the class of naphthyridine derivatives. It features a chlorine atom at the 5th and 7th positions of the naphthyridin-4-one ring, which contributes to its unique structural features and potential applications in medicinal chemistry.

863785-66-4

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863785-66-4 Usage

Uses

Used in Pharmaceutical Industry:
5,7-DICHLORO-1H-[1,6]NAPHTHYRIDIN-4-ONE is used as a building block for the synthesis of other biologically active compounds due to its potential biological activities. Its unique structural features make it a promising candidate for the development of pharmaceutical drugs, particularly in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 863785-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,8 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 863785-66:
(8*8)+(7*6)+(6*3)+(5*7)+(4*8)+(3*5)+(2*6)+(1*6)=224
224 % 10 = 4
So 863785-66-4 is a valid CAS Registry Number.

863785-66-4Relevant academic research and scientific papers

PYRIDO-AZAHETERECYDIC COMPOUND AND PREPARATION METHOD AND USE THEREOF

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Paragraph 0095-0096, (2018/09/21)

The present invention discloses a pyrido-azacyclic compound represented by formula I, an isomer thereof, a pharmaceutically acceptable salt or a pharmaceutically acceptable solvate thereof, a preparation process thereof and a composition comprising the compound, and a use thereof as a multi-target protein kinase inhibitor in the preparation of a medicament for the treatment of diseases that are associated with protein kinase, especially c-Met, such as cancer and the like. The compound represented by formula I has potent inhibitory activity on tumor cells with overexpression of c-Met kinase, can effectively target c-Met-mediated signaling pathway, and can be used in the treatment of diseases such as cancer and the like that is caused by the overexpression of c-Met kinase.

Strategic studies in the syntheses of novel 6,7-substituted quinolones and 7- or 6-substituted 1,6- and 1,7-naphthyridones

Morgentin, Rémy,Pasquet, Georges,Boutron, Pascal,Jung, Frédéric,Lamorlette, Maryannick,Maudet, Micka?l,Plé, Patrick

, p. 2772 - 2782 (2008/09/19)

This paper describes the different strategies devised and applied to overcome the selectivity issues in the syntheses of 6,7-disubstituted-1H-quinolin-4-one, 7-substituted-1H-1,6-naphthyridin-4-one and 6-substituted-1H-1,7-naphthyridin-4-one derivatives. They allowed us to improve the overall yields and the scaling-up feasibility. Several examples illustrate these strategies with their advantages and drawbacks.

NAPHTHYRIDINE DERIVATIVES AS ANTI-CANCER AGENTS

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Page/Page column 97, (2010/11/28)

The invention concerns naphthyridine derivatives of Formula (I): or a pharmaceutically-acceptable salt thereof, wherein each of X1, p, R1, G1, G2, q, R2, R3, R4, R5, Ring A, r and R6 has any of the meanings defined hereinbefore in the description; pharmaceutical compositions containing them and their use in the treatment of cell proliferative disorders or disease states associated with angiogenesis and/or vascular permeability.

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