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6-AMINO-(1H)INDAZOLE-3-CARBOXYLIC ACID is an amino and carboxyl substituted indazole derivative that serves as a building block in various synthetic preparations. It is an analogue of Indazole-3-carboxylic Acid (I505000), which is known for its potential in treating pain and inflammation.

885519-22-2

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885519-22-2 Usage

Uses

Used in Pharmaceutical Industry:
6-AMINO-(1H)INDAZOLE-3-CARBOXYLIC ACID is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential applications in treating pain and inflammation.
Used in Research and Development:
6-AMINO-(1H)INDAZOLE-3-CARBOXYLIC ACID is utilized in research and development for the creation of novel indazole-based compounds. Its properties as an analogue of Indazole-3-carboxylic Acid make it a valuable tool for exploring new therapeutic agents and understanding their mechanisms of action.
Used in Drug Design and Synthesis:
6-AMINO-(1H)INDAZOLE-3-CARBOXYLIC ACID is employed in drug design and synthesis processes to create new chemical entities with potential therapeutic benefits. Its versatility as a building block enables the development of innovative drugs targeting various medical conditions, including pain and inflammation.

Check Digit Verification of cas no

The CAS Registry Mumber 885519-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,1 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 885519-22:
(8*8)+(7*8)+(6*5)+(5*5)+(4*1)+(3*9)+(2*2)+(1*2)=212
212 % 10 = 2
So 885519-22-2 is a valid CAS Registry Number.

885519-22-2Downstream Products

885519-22-2Relevant academic research and scientific papers

2-AMINOQUINAZOLINE DERIVATIVE

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Page/Page column 55-56, (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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