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38186-86-6

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38186-86-6 Usage

Description

6-Chloro-5-fluoro-nicotinic acid is a chemical compound with the molecular formula C6H3ClFNO2, belonging to the class of nicotinic acid derivatives. It is characterized by the presence of both chlorine and fluorine atoms, which contribute to its unique chemical and biological properties. 6-Chloro-5-fluoro-nicotinic acid serves as a valuable building block in the synthesis of various pharmaceutical agents and intermediates, and has been studied for its potential biological and pharmacological properties. Its versatile structure and functional groups make it a promising candidate for the development of novel drugs with improved pharmacokinetic and pharmacodynamic profiles.

Uses

Used in Pharmaceutical Industry:
6-Chloro-5-fluoro-nicotinic acid is used as a key building block for the synthesis of various pharmaceutical agents and intermediates. Its presence in the molecular structure of these agents allows for the development of drugs with enhanced pharmacological properties, such as increased potency, selectivity, and bioavailability.
Used in Drug Development:
6-Chloro-5-fluoro-nicotinic acid is utilized as a starting material for the development of novel drugs with improved pharmacokinetic and pharmacodynamic properties. The presence of both chlorine and fluorine atoms in the molecule enables the design of drugs with better absorption, distribution, metabolism, and excretion profiles, leading to more effective therapeutic outcomes.
Used in Agrochemicals:
6-Chloro-5-fluoro-nicotinic acid has been investigated for its potential applications in agrochemicals. Its unique chemical properties and reactivity make it a promising candidate for the development of new agrochemicals with improved efficacy and selectivity, contributing to more sustainable agricultural practices.
Used in Material Science:
6-Chloro-5-fluoro-nicotinic acid has also been explored for its potential applications in material science. Its chemical and physical properties, such as its reactivity and stability, make it a valuable component in the development of new materials with specific properties, such as improved mechanical strength, thermal stability, or electrical conductivity.

Check Digit Verification of cas no

The CAS Registry Mumber 38186-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,8 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38186-86:
(7*3)+(6*8)+(5*1)+(4*8)+(3*6)+(2*8)+(1*6)=146
146 % 10 = 6
So 38186-86-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClFNO2/c7-5-4(8)1-3(2-9-5)6(10)11/h1-2H,(H,10,11)

38186-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-5-fluoropyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Carboxy-6-chloro-5-fluoropyridine

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:38186-86-6 SDS

38186-86-6Relevant articles and documents

DIHYDROPYRIMIDINE DERIVATIVES AND USES THEREOF IN THE TREATMENT OF HBV INFECTION OR OF HBV-INDUCED DISEASES

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Page/Page column 39; 255-256, (2020/01/24)

The application describes dihydropyrimidine derivatives which are useful in the treatment or prevention of HBV infection or of HBV-induced diseases, more particularly of HBV chronic infection or of diseases induced by HBV chronic infection, as well as pharmaceutical or medical applications thereof.

BIS-(SULFONYLAMINO) DERIVATIVES FOR TREATMENT OF PAIN AND INFLAMMATION

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Page/Page column 91, (2010/12/17)

The invention provides compounds of formula (I) wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together

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