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2,8-Dichloro-quinazoline, a quinazoline derivative with the molecular formula C8H5Cl2N3, is a heterocyclic compound characterized by a benzene ring fused to a pyrimidine ring. It is recognized for its potential in the synthesis of various drugs and biologically active compounds, as well as its antimicrobial and anticancer properties, positioning it as a valuable compound in medicinal chemistry research.

67092-20-0

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67092-20-0 Usage

Uses

Used in Pharmaceutical Industry:
2,8-Dichloro-quinazoline is used as a building block for the synthesis of various drugs and biologically active compounds, contributing to the development of new therapeutic agents.
Used in Research and Development:
In the realm of research and development, 2,8-Dichloro-quinazoline serves as a starting material for the synthesis of new potential drug candidates, facilitating the discovery of innovative treatments and pharmaceuticals.
Used in Medicinal Chemistry Research:
2,8-Dichloro-quinazoline is used as a subject of interest in medicinal chemistry research due to its potential antimicrobial and anticancer properties, which could lead to the creation of novel treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 67092-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67092-20:
(7*6)+(6*7)+(5*0)+(4*9)+(3*2)+(2*2)+(1*0)=130
130 % 10 = 0
So 67092-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H4Cl2N2/c9-6-3-1-2-5-4-11-8(10)12-7(5)6/h1-4H

67092-20-0Relevant academic research and scientific papers

Substituted piperazine compounds, application method and applications thereof

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Paragraph 0223; 0224; 0225, (2016/10/09)

The invention discloses substituted piperazine compounds, an application method and applications thereof. Specifically, the invention relates to piperazine compounds and pharmaceutical compositions thereof for inhibiting reuptake of 5-hydroxytryptamine and/or stimulation of 5-HT1A acceptor. The invention also relates to a preparation method of the compounds and pharmaceutical compositions thereof, and an application of the compounds and pharmaceutical compositions thereof in the treatment of central nervous system dysfunction.

Novel Mps1 kinase inhibitors: From purine to pyrrolopyrimidine and quinazoline leads

Bursavich, Matthew G.,Dastrup, David,Shenderovich, Mark,Yager, Kraig M.,Cimbora, Daniel M.,Williams, Brandi,Kumar, D. Vijay

, p. 6829 - 6833 (2014/01/06)

Mps1, also known as TTK, is a mitotic checkpoint protein kinase that has become a promising new target of cancer research. In an effort to improve the lead-likeness of our recent Mps1 purine lead compounds, a scaffold hopping exercise has been undertaken.

NITROGEN HETEROCYCLIC COMPOUNDS USEFUL AS PDE10 INHIBITORS

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Page/Page column 185, (2011/12/02)

Unsaturated nitrogen heterocyclic compounds of formula (I): (I), as defined in the specification, compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, Huntington's Disease, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.

2-AMINOQUINAZOLINE DERIVATIVE

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Page/Page column 34, (2010/09/17)

An object of the present invention is to provide compounds which are useful as protein kinase inhibitors. Disclosed is a 2-aminoquinazoline derivative represented by the following formula (I): wherein R1 represents a lower alkyl group which may be substituted with a halogen atom, or a halogen atom; R2 represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, a halogen atom, a hydroxyl group, a substituted or unsubstituted lower alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted acylamino group, a carboxyl group, a lower alkoxycarbonyl group, a carbamoyl group, or a substituted or unsubstituted lower alkylureido group; and X, Y and Z each independently represents a hydrogen atom, a substituted or unsubstituted lower alkyl group, a halogen atom, a hydroxyl group, a carboxyl group, a lower alkoxycarbonyl group, a cyano group, a carbamoyl group, a substituted or unsubstituted lower alkoxy group, a substituted or unsubstituted amino group, a substituted or unsubstituted lower alkoxycarbonylamino group, a substituted or unsubstituted lower alkylaminocarbonyl group, a lower alkylsulfonylamino group, a substituted or unsubstituted lower alkylureido group, or a substituted or unsubstituted acylamino group, or X and Y may be combined to form a 5- to 6-membered ring forming a bicyclic fused ring, wherein the 5- to 6-membered ring may optionally have a substituent, provided that when X and Y are not combined to form a fused ring, R2 represents a hydrogen atom and, when X and Y are combined to form a fused ring, a saturated or unsaturated, bicyclic alicyclic or heterocyclic fused ring can be formed.

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