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6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is a quinoline derivative with the molecular formula C16H10BrNO2S, featuring a thiophene ring, a carboxylic acid group, and a bromine atom at the 6-position. This chemical compound is recognized for its potential as an anti-cancer and anti-inflammatory agent, and its unique structure and functional groups contribute to its versatility and value in scientific and industrial applications.

33289-49-5

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33289-49-5 Usage

Uses

Used in Pharmaceutical Research:
6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as a building block in pharmaceutical research for its potential as an anti-cancer and anti-inflammatory agent. Its unique structure allows for the development of new drugs targeting various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, 6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as a key intermediate for the synthesis of various complex organic compounds. Its functional groups enable it to participate in a wide range of chemical reactions, making it a valuable component in the creation of novel molecules.
Used in Chemical Research:
6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is utilized in chemical research to study its properties and explore its potential applications. Its unique structure and functional groups make it an interesting subject for investigation, which can lead to new discoveries and advancements in the field of chemistry.
Used in Drug Development:
6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used in drug development as a potential therapeutic agent. Its anti-cancer and anti-inflammatory properties are being investigated for the treatment of various diseases, with the aim of developing new and effective medications.
Used in Industrial Applications:
In industrial applications, 6-BROMO-2-THIOPHEN-2-YL-QUINOLINE-4-CARBOXYLIC ACID is used as a versatile chemical compound for the production of various products. Its unique structure and functional groups make it suitable for use in a wide range of industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 33289-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,2,8 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33289-49:
(7*3)+(6*3)+(5*2)+(4*8)+(3*9)+(2*4)+(1*9)=125
125 % 10 = 5
So 33289-49-5 is a valid CAS Registry Number.

33289-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-thiophen-2-ylquinoline-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-bromo-2-thien-2-ylquinoline-4-carboxylic acid

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:33289-49-5 SDS

33289-49-5Downstream Products

33289-49-5Relevant academic research and scientific papers

Heterocyclic Diamidine DNA Ligands as HOXA9 Transcription Factor Inhibitors: Design, Molecular Evaluation, and Cellular Consequences in a HOXA9-Dependant Leukemia Cell Model

Depauw, Sabine,Lambert, Mélanie,Jambon, Samy,Paul, Ananya,Peixoto, Paul,Nhili, Raja,Marongiu, Laura,Figeac, Martin,Dassi, Christelle,Paul-Constant, Charles,Billoré, Benjamin,Kumar, Arvind,Farahat, Abdelbasset A.,Ismail, Mohamed A.,Mineva, Ekaterina,Sweat, Daniel P.,Stephens, Chad E.,Boykin, David W.,Wilson, W. David,David-Cordonnier, Marie-Hélène

, p. 1306 - 1329 (2019/02/14)

Most transcription factors were for a long time considered as undruggable targets because of the absence of binding pockets for direct targeting. HOXA9, implicated in acute myeloid leukemia, is one of them. To date, only indirect targeting of HOXA9 expres

Synthesis and pharmacological properties of some quinoline derivatives

Kalluraya, Balakrishna,Sreenivasa

, p. 399 - 404 (2007/10/03)

A series of 2-(2-thienyl)cinchoninic acids 3, their derivatives 5 and 4-(3-substituted-1,2,4-triazolo[3,4-b]- 1,3,4-thiaziazolo-6-yl)-2-(2-thienyl)quinolines 6 were synthesized. The structures of the newly synthesized compounds are confirmed by analytical, IR, NMR and mass spectral data. The newly synthesized compounds were evaluated for their anti-inflammatory, analgesic and anthelmintic activity. The results indicated that dinitrothiophene derivatives 5 are more active.

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