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6-Bromo-3-phenyl-1H-indazole is a chemical compound that belongs to the group of indazoles, which are nitrogen-containing aromatic heterocycles. It has a molecular formula of C14H9BrN2 and a molar mass of 295.14 g/mol. The molecule consists of a phenyl ring attached at position three and a bromine atom at position six on the indazole skeleton. 6-BROMO-3-PHENYL-1H-INDAZOLE is significant in organic and medicinal chemistry due to its incorporation into many pharmaceutical drugs. However, detailed information on its specific toxicity, safety, or environmental effects are relatively scarce, and more research is required to fully understand its various effects and potential applications.

885271-16-9

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885271-16-9 Usage

Uses

Used in Pharmaceutical Industry:
6-Bromo-3-phenyl-1H-indazole is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique chemical structure allows for the development of new drug candidates with potential therapeutic applications.
Used in Organic Chemistry Research:
6-Bromo-3-phenyl-1H-indazole is used as a building block in the synthesis of complex organic molecules. Its reactivity and structural features make it a valuable compound for exploring new chemical reactions and pathways.
Used in Medicinal Chemistry:
6-Bromo-3-phenyl-1H-indazole is used as a scaffold in the design of new drug molecules. Its incorporation into drug candidates can potentially lead to the discovery of novel therapeutic agents with improved efficacy and safety profiles.
Note: The specific applications mentioned above are hypothetical and based on the general properties of 6-Bromo-3-phenyl-1H-indazole. More research and development are needed to validate these applications and understand the compound's full potential in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 885271-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885271-16:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*1)+(2*1)+(1*6)=199
199 % 10 = 9
So 885271-16-9 is a valid CAS Registry Number.

885271-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-3-phenyl-1H-indazole

1.2 Other means of identification

Product number -
Other names 6-BROMO-3-PHENYL-1H-INDAZOLE

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:885271-16-9 SDS

885271-16-9Relevant academic research and scientific papers

Copper-Promoted Oxidative Intramolecular C–H Amination of Hydrazones to Synthesize 1H-Indazoles and 1H-Pyrazoles Using a Cleavable Directing Group

Zhang, Guofu,Fan, Qiankun,Zhao, Yiyong,Ding, Chengrong

supporting information, p. 5801 - 5806 (2019/08/02)

A facile and efficient synthesis of 1H-indazoles and 1H-pyrazoles through a copper-promoted oxidative intramolecular C–H amination of hydrazones using a cleavable directing group was developed. This reaction is characterized by its mild conditions, operational simplicity, readily available reagents, and excellent yields. A tentative mechanism for Cu-mediated C–H oxidative amination was proposed.

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

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Page/Page column 123, (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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