1107694-84-7

Usage

Uses

Due to the limited information available about 2,8-Dichloroquinazolin-4-aMine, its specific applications are not well-defined. However, based on its chemical structure and the general properties of quinazolines, potential uses may include:
Used in Pharmaceutical Industry:
2,8-Dichloroquinazolin-4-aMine could be used as a building block or intermediate in the synthesis of various pharmaceutical compounds, given the presence of the quinazoline moiety, which is a common structural element in many bioactive molecules.
Used in Chemical Research:
As a member of the quinazoline class, 2,8-Dichloroquinazolin-4-aMine may be utilized in chemical research to explore its reactivity, potential for forming new compounds, and its properties in various chemical reactions.
Used in Material Science:
2,8-Dichloroquinazolin-4-aMine's unique structure and functional groups may offer potential applications in the development of new materials with specific properties, such as in the field of organic electronics or as a component in advanced materials.

Upstream product

• 62484-29-1 2,4,8-trichloroquinazoline 

Downstream Products

• 67092-20-0 2,8-dichloroquinazoline 

Relevant academic research and scientific papers

2-AMINOQUINAZOLINE DERIVATIVE

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.