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2,8-Bromo-1,5-naphthyridine, with the molecular formula C8H5BrN2, is a brominated naphthyridine derivative that serves as a versatile building block in the realms of organic synthesis and medicinal chemistry. Characterized by its unique structure and reactivity, 2,8-BroMo-1,5-naphthyridine is recognized for its potential applications in the development of pharmaceuticals, agrochemicals, and materials for a variety of industrial uses. Its intriguing biological activities have placed it under scrutiny for its possible roles as an anti-cancer agent, anti-inflammatory, and antimicrobial, making it a promising candidate for the creation of innovative chemical entities with therapeutic potential.

1363380-58-8

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1363380-58-8 Usage

Uses

Used in Pharmaceutical Development:
2,8-Bromo-1,5-naphthyridine is utilized as a key intermediate in the synthesis of various pharmaceutical compounds due to its potential to contribute to the development of new drugs with enhanced therapeutic properties. Its unique chemical structure allows for the design of molecules that can target specific biological pathways, offering a broad range of applications in medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 2,8-Bromo-1,5-naphthyridine is employed as a precursor in the synthesis of novel agrochemicals, including pesticides and herbicides. Its incorporation into these products can lead to the development of more effective and environmentally friendly solutions for agricultural challenges.
Used in Material Science:
2,8-Bromo-1,5-naphthyridine is also used as a component in the creation of advanced materials for industrial applications. Its unique chemical properties can be leveraged to produce materials with specific characteristics, such as improved stability, reactivity, or selectivity, which can be beneficial in various industrial processes.
Used in Anticancer Research:
2,8-Bromo-1,5-naphthyridine is studied for its potential as an anti-cancer agent, where it may be used to develop compounds that target and inhibit the growth of cancer cells. Its biological activity makes it a valuable tool in the ongoing search for new and effective treatments for various types of cancer.
Used in Anti-Inflammatory and Antimicrobial Agents:
2,8-BroMo-1,5-naphthyridine is also being explored for its anti-inflammatory and antimicrobial properties, suggesting its use in the development of new therapeutic agents to combat inflammation and infectious diseases. Its potential in these areas highlights the versatility of 2,8-Bromo-1,5-naphthyridine in addressing diverse medical needs.

Check Digit Verification of cas no

The CAS Registry Mumber 1363380-58-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,3,8 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1363380-58:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*8)+(3*0)+(2*5)+(1*8)=158
158 % 10 = 8
So 1363380-58-8 is a valid CAS Registry Number.

1363380-58-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,8-dibromo-1,5-naphthyridine

1.2 Other means of identification

Product number -
Other names 2,8-BROMO-1,5-NAPHTHYRIDINE

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:1363380-58-8 SDS

1363380-58-8Downstream Products

1363380-58-8Relevant academic research and scientific papers

NITROGEN-CONTAINING HETEROCYCLIC COMPOUND OR SALT THEREOF

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Paragraph 0465; 0466; 0467, (2015/11/30)

A compound represented by Formula [1] (in the formula, Z1 represents N, CH, or the like; X1 represents NH or the like; R1 represents a heteroaryl group or the like; each of R2, R3, and R4 represents a hydrogen atom, a halogen atom, an alkoxy group, or the like; and R5 represents a heteroaryl group or the like) or salt thereof.

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