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3,7-Dibromo-1,5-naphthyridine is a halogenated naphthyridine derivative with the molecular formula C8H4Br2N2. It is a valuable building block in organic synthesis, known for its high reactivity and ability to participate in a variety of chemical reactions. This chemical compound is used in the synthesis of various pharmaceuticals and agrochemicals, making it a versatile tool for the creation of novel chemical compounds with potential therapeutic or agricultural uses.

17965-72-9

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17965-72-9 Usage

Uses

Used in Pharmaceutical Industry:
3,7-Dibromo-1,5-naphthyridine is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to create a wide range of functionalized naphthyridine derivatives with diverse applications. Its high reactivity allows for the development of new drugs with potential therapeutic uses.
Used in Agrochemical Industry:
3,7-Dibromo-1,5-naphthyridine is used as a starting material in the synthesis of agrochemicals, contributing to the development of novel compounds with potential applications in agriculture. Its versatility in chemical reactions enables the creation of new agrochemicals with improved properties and effectiveness.
Used in Organic Synthesis:
3,7-Dibromo-1,5-naphthyridine is used as a valuable building block in organic synthesis for its ability to participate in a variety of chemical reactions. This allows chemists to create new functionalized naphthyridine derivatives with potential applications in various fields, including pharmaceuticals, agrochemicals, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 17965-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17965-72:
(7*1)+(6*7)+(5*9)+(4*6)+(3*5)+(2*7)+(1*2)=149
149 % 10 = 9
So 17965-72-9 is a valid CAS Registry Number.

17965-72-9SDS

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 3,7-Dibromo-1,5-naphthyridine

1.2 Other means of identification

Product number -
Other names 3,7-Dibrom-1,5-naphthyridin

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:17965-72-9 SDS

17965-72-9Upstream product

17965-72-9Downstream Products

17965-72-9Relevant academic research and scientific papers

Synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid

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Paragraph 0057; 0058; 0059, (2018/11/03)

The invention provides a synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid. The synthetic method of the 2-bromo-1,5-naphthyridine-3-methanoic acid comprises the steps of taking 1,5-naphthyridine as a raw material and reacting to generate 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate; and finally hydrolyzing the 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate under thealkaline condition to generate the 7-bromo-1,5-naphthyridine-3-methanoic acid. According to the synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid, a synthetic route which takes 1,5-naphthyridine as a raw material is provided. The synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid has the advantages that the synthetic route is simple, the raw materials are low in cost, are simple and are easily obtained, aftertreatment is facilitated, the success rate is high, the synthetic route is easy to enlarge and the like.

SUBSTITUTED NAPHTHYRIDINE AND QUINOLINE COMPOUNDS AS MAO INHIBITORS

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Paragraph 0370; 0371, (2014/09/30)

The invention provides a chemical entity of Formula (I) wherein R1, R2, R3, Y, and n have any of the values described herein and compositions comprising such chemical entities; methods of making them; and their use in a wi

Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists

Galatsis, Paul,Yamagata, Koji,Wendt, John A.,Connolly, Cleo J.,Mickelson, John W.,Milbank, Jared B.J.,Bove, Susan E.,Knauer, Christopher S.,Brooker, Rachel M.,Augelli-Szafran, Corinne E.,Schwarz, Roy D.,Kinsora, Jack J.,Kilgore, Kenneth S.

, p. 6525 - 6528 (2008/03/18)

We describe three novel regioisomeric series of aryl naphthyridine analogs, which are potent antagonists of the Class III GPCR mGlu5 receptor. The synthesis and in vitro and in vivo pharmacological activities of these analogs are discussed.

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