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Ethanone, 1-(6-bromo-1H-indazol-1-yl)-, is a chemical compound that features an ethanone group connected to a 1-(6-bromo-1H-indazol-1-yl) moiety. It is a member of the indazole class, which is a group of heterocyclic compounds characterized by a fused ring structure with nitrogen and carbon atoms. The presence of a bromine atom at the 6-position of the indazole ring endows the molecule with unique chemical and physical attributes, which may be valuable in research and various industrial applications. Ethanone, 1-(6-broMo-1H-indazol-1-yl)could also possess pharmacological properties that warrant investigation in the context of drug discovery and development. Further research is required to fully elucidate its characteristics and potential applications.

651780-33-5

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651780-33-5 Usage

Uses

Used in Pharmaceutical Research:
Ethanone, 1-(6-bromo-1H-indazol-1-yl)is utilized as a chemical intermediate in the development of new pharmaceuticals, particularly for its potential pharmacological activities. Its unique structure may offer novel avenues for drug discovery, including the design of new therapeutic agents.
Used in Chemical Synthesis:
In the chemical industry, Ethanone, 1-(6-bromo-1H-indazol-1-yl)serves as a key building block for the synthesis of more complex organic compounds. Its reactivity and structural features make it a valuable component in the creation of advanced materials and specialty chemicals.
Used in Material Science:
Ethanone, 1-(6-bromo-1H-indazol-1-yl)may also find applications in material science, where its specific chemical and physical properties could contribute to the development of new materials with tailored properties for various uses, such as in electronics, coatings, or sensors.

Check Digit Verification of cas no

The CAS Registry Mumber 651780-33-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,7,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 651780-33:
(8*6)+(7*5)+(6*1)+(5*7)+(4*8)+(3*0)+(2*3)+(1*3)=165
165 % 10 = 5
So 651780-33-5 is a valid CAS Registry Number.

651780-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-bromoindazol-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1H-Indazole,1-acetyl-6-bromo

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:651780-33-5 SDS

651780-33-5Downstream Products

651780-33-5Relevant academic research and scientific papers

Protected indazole boronic acid pinacolyl esters: Facile syntheses and studies of reactivities in Suzuki-Miyaura cross-coupling and hydroxydeboronation reactions

Crestey, Fran?ois,Lohou, Elodie,Stiebing, Silvia,Collot, Valérie,Rault, Sylvain

body text, p. 615 - 619 (2009/07/09)

The paper describes a rapid and efficient synthesis for the isolation of protected indazolylboronic esters. These compounds were synthesized by reaction between prepared protected haloindazoles and bis(pinacolato)diboron. The effects of solvent, temperature, reaction time, and the nature of halogen atom as well as protecting group were investigated. Additionaly, these compounds reacted either with aryl halides in a Suzuki-Miyaura cross-coupling reaction or with hydrogen peroxide in a hydroxydeboronation reaction showing the potential access to new aryl and hydroxyindazole libraries. Georg Thieme Verlag Stuttgart.

6' SUBSTITUTED COMPOUNDS HAVING 5-HT6 RECEPTOR AFFINITY

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Page/Page column 34; 35, (2008/12/08)

The present disclosure provides compounds having affinity for the 5-HT6 receptor which are of the formula (I): wherein R1—R4 A, B, D, E, and G are as defined herein. The disclosure also relates to methods of preparing such compounds, compositions containing such compounds, and methods of use thereof.

FUSED HETEROARYL DERIVATIVES FOR USE AS P38 KINASE INHIBITORS IN THE TREATMENT OF I.A. RHEUMATOID ARTHRISTIS

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Page/Page column 54, (2010/11/30)

Compounds of formula (I): wherein A is a 5-membered heteroaryl ring are inhibitors of p38 kinase and are useful in the treatment of conditions or disease states mediated by p38 kinase activity or mediated by cytokines produced by the activity of p38, such as rheumatoid arthritis.

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