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ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE, a chemical compound with the molecular formula C9H9NO3, is a pyridine derivative known for its antioxidant and anti-inflammatory properties. It is a clear, colorless liquid with a characteristic odor, typically handled in a controlled laboratory setting due to its potential health hazards. ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE is commonly used in the synthesis of pharmaceuticals and agrochemicals, and its potential therapeutic benefits make it a valuable asset in various applications.

53389-00-7

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53389-00-7 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE is used as an intermediate in the synthesis of various pharmaceuticals for its antioxidant and anti-inflammatory properties, which can contribute to the development of drugs with therapeutic benefits.
Used in Agrochemical Industry:
ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE is used as a precursor in the production of agrochemicals, where its properties can be harnessed to create compounds that protect crops and enhance agricultural productivity.
Used in Cosmetic Industry:
ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE is used as an active ingredient in cosmetic formulations for its antioxidant properties, which can help protect the skin from environmental damage and promote a healthier appearance.
Used in Research and Development:
ETHYL 6-HYDROXYPYRIDINE-2-CARBOXYLATE is used as a research compound in the development of new chemical entities and the study of its potential applications in various fields, including medicine, agriculture, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 53389-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,8 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53389-00:
(7*5)+(6*3)+(5*3)+(4*8)+(3*9)+(2*0)+(1*0)=127
127 % 10 = 7
So 53389-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO3/c1-2-12-8(11)6-4-3-5-7(10)9-6/h3-5H,2H2,1H3,(H,9,10)

53389-00-7SDS

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 Ethyl 6-hydroxypyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 6-oxo-1H-pyridine-2-carboxylate

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:53389-00-7 SDS

53389-00-7Downstream Products

53389-00-7Relevant academic research and scientific papers

TRIAZOLOPYRIMIDINE DERIVATIVES FOR USE AS GHRELIN O-ACYL TRANSFERASE (GOAT) INHIBITORS

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Page/Page column 62, (2019/08/26)

The present invention relates to compounds of general formula I, wherein the groups R1 and R2 are defined as in claim 1, which have valuable pharmacological properties, in particular bind to ghrelin O-acyl transferase (GOAT) and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular obesity.

ARYLHYDRAZIDES CONTAINING A 2-PYRIDONE MOIETY AS SELECTIVE ANTIBACTERIAL AGENTS

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Page/Page column 42, (2016/03/12)

The present invention belongs to the field of antibacterial agents, more specifically to antibacterials for treating Acinetobacter baumannii infections. The invention provides arylhydrazides containing a 2-pyridone moiety, according to formula (I), which

An annulation method for the synthesis of alkyl-substituted 6-carbomethoxy-2-pyridones

Zhang, Yu,Loertscher, Brad M.,Castle, Steven L.

experimental part, p. 6584 - 6590 (2011/02/25)

A protocol for the synthesis of 5-alkyl and 3,5-dialkyl-6-carbomethoxy-2-pyridones was devised. Key steps include a Mannich reaction, acylation of a tosylamine, and a PPh3/TiCl4-promoted intramolecular Reformatsky-type reaction with

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