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4-Amino-6-bromoquinoline is a heterocyclic aromatic compound with the molecular formula C9H7BrN2, featuring a quinoline backbone. It is widely recognized for its potential as an intermediate in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals.

65340-73-0

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65340-73-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Amino-6-bromoquinoline is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of drugs with diverse therapeutic properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 4-Amino-6-bromoquinoline serves as a key intermediate, aiding in the creation of compounds designed to protect crops and enhance agricultural productivity.
Used as Antimalarial Agent:
4-Amino-6-bromoquinoline is utilized as an antimalarial agent, leveraging its chemical structure to combat the Plasmodium parasites responsible for malaria.
Used as Antituberculosis Agent:
In the fight against tuberculosis, 4-Amino-6-bromoquinoline is applied as an antituberculosis agent, potentially contributing to the treatment of this infectious disease by targeting Mycobacterium tuberculosis.
Used as Antiviral Agent:
4-Amino-6-bromoquinoline also sees use as an antiviral agent, where its unique structure may help in the development of treatments for viral infections.
Used in Dye Synthesis:
4-Amino-6-bromoquinoline is used as a building block in the synthesis of dyes, capitalizing on its chemical properties to create a range of colorants for various applications.
Used in Fluorescent Probes:
It is also utilized in the development of fluorescent probes, important for biological and chemical research, taking advantage of its ability to emit light upon interaction with specific substances.
Used in Material Science:
Furthermore, 4-Amino-6-bromoquinoline is a valuable component in material science, employed in the synthesis of new materials and compounds for a wide array of industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65340-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,4 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65340-73:
(7*6)+(6*5)+(5*3)+(4*4)+(3*0)+(2*7)+(1*3)=120
120 % 10 = 0
So 65340-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrN2/c10-6-1-2-9-7(5-6)8(11)3-4-12-9/h1-5H,(H2,11,12)

65340-73-0 Well-known Company Product Price

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  • Aldrich

  • (BBO000153)  4-Amino-6-bromoquinoline  AldrichCPR

  • 65340-73-0

  • BBO000153-1G

  • 2,901.60CNY

  • Detail

65340-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-6-bromoquinoline

1.2 Other means of identification

Product number -
Other names 6-bromoquinolin-4-amine

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:65340-73-0 SDS

65340-73-0Upstream product

65340-73-0Relevant academic research and scientific papers

Synthesis and evaluation of sulfonamide derivatives as potent Human Uric Acid Transporter 1 (hURAT1) inhibitors

Yang, Xintuo,Pang, Xuehai,Fan, Lei,Li, Xinghai,Chen, Yuanwei

supporting information, p. 1919 - 1922 (2017/04/10)

This letter presents synthesis and structure-activity relationship study of sulfonamide derivatives as inhibitors of Human Uric Acid Transporter 1 (hURAT1). Among all tested sulfonamide derivatives, compounds 9b, 16i and 19b exhibited excellent inhibition activity with IC50 value of 10, 2, and 83?nM, respectively. In addition, compounds 9b and 19b demonstrated moderate PK profile in rats.

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