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6-Methy-1H-indazol-5-ol is a chemical compound belonging to the indazole class, characterized by a benzene ring fused to a pyrazole ring. With the chemical formula C9H9N3O, it consists of nine carbon, nine hydrogen, three nitrogen, and one oxygen atoms. This complex compound is primarily utilized in medicinal chemistry and drug discovery due to the biological activity of its indazole derivatives. However, detailed information on its toxicity, ecological impact, and experimental properties may be limited, necessitating careful handling and standard precautionary measures.

478832-60-9

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478832-60-9 Usage

Uses

Used in Medicinal Chemistry:
6-Methy-1H-indazol-5-ol is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential biological activity. Its unique structure allows for the development of new drugs with specific therapeutic targets.
Used in Drug Discovery:
In the field of drug discovery, 6-Methy-1H-indazol-5-ol serves as a valuable scaffold for the design and optimization of novel therapeutic agents. Its indazole core can be modified to enhance the potency, selectivity, and pharmacokinetic properties of the resulting drug candidates.
Used in Chemical Research:
6-Methy-1H-indazol-5-ol is also employed in chemical research to explore the reactivity and functionalization of indazole derivatives. This helps in understanding the structure-activity relationships and the potential applications of these compounds in various chemical and biological processes.
Used in Organic Synthesis:
As an organic compound, 6-Methy-1H-indazol-5-ol can be used in various organic synthesis reactions, such as cross-coupling, oxidation, and reduction, to generate a diverse range of indazole-based molecules with different functional groups and properties.
Used in Material Science:
Although not explicitly mentioned in the provided materials, 6-Methy-1H-indazol-5-ol may also find applications in material science, such as in the development of novel organic materials with specific electronic, optical, or magnetic properties, based on the indazole core.

Check Digit Verification of cas no

The CAS Registry Mumber 478832-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,8,3 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 478832-60:
(8*4)+(7*7)+(6*8)+(5*8)+(4*3)+(3*2)+(2*6)+(1*0)=199
199 % 10 = 9
So 478832-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O/c1-5-2-7-6(3-8(5)11)4-9-10-7/h2-4,11H,1H3,(H,9,10)

478832-60-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxy-6-methyl-1H-indazole

1.2 Other means of identification

Product number -
Other names 6-Methyl-1H-indazol-5-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:478832-60-9 SDS

478832-60-9Relevant academic research and scientific papers

MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-κB ACTIVITY AND USE THEREOF

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Page/Page column 112, (2008/12/05)

Novel non-steroidal compounds are provided which are useful in treating diseases associated with modulation of the glucocorticoid receptor, and/or AP-1, and/or NF-κB activity including inflammatory and immune diseases, obesity and diabetes having the structure of formula (I), its enantiomers, diastereomers, or a pharmaceutically-acceptable salt, or hydrate, thereof, wherein (Ia) is heterocycle or heteroaryl; J, Ja, E, F, G, Ma, M, Q, Za and Z are as defined herein. Also provided are pharmaceutical compositions and methods of treating inflammatory- or immune-associated diseases and obesity and diabetes employing said compounds.

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