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1-(2-HYDROXY-ETHYL)-1H-INDAZOL-6-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

874668-60-7

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874668-60-7 Usage

Class

Indazoles
It belongs to a class of heterocyclic compounds containing a six-membered ring with two nitrogen atoms and one carbon atom.

Structure

Indazole ring with a hydroxy-ethyl group attached
The compound features an indazole ring, which is a fused pyrazole and pyridine ring system, with an additional hydroxy-ethyl group.

Organic compound

Yes
It is an organic compound, meaning it primarily consists of carbon and hydrogen atoms.

Pharmaceutical research and development

Commonly used
The compound is frequently utilized in the field of pharmaceutical research and development.

Synthesis

Potential drug candidates
It is used in the synthesis of potential drug candidates, indicating its potential for therapeutic applications.

Properties

Promising for further study
The compound's properties and potential biological activities make it a molecule of interest for further study in the medical and pharmaceutical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 874668-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,6,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 874668-60:
(8*8)+(7*7)+(6*4)+(5*6)+(4*6)+(3*8)+(2*6)+(1*0)=227
227 % 10 = 7
So 874668-60-7 is a valid CAS Registry Number.

874668-60-7Relevant academic research and scientific papers

1-((S)-2-aminopropyl)-1H-indazol-6-ol: A potent peripherally acting 5-HT2 receptor agonist with ocular hypotensive activity

May, Jesse A.,Dantanarayana, Anura P.,Zinke, Paul W.,McLaughlin, Marsha A.,Sharif, Najam A.

, p. 318 - 328 (2006)

Serotonin 5-HT2 receptor agonists have been identified as a potential new class of agents for the treatment of ocular hypertension and glaucoma. The initially reported tryptamine analogues displayed either poor solution stability, potent centra

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