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243977-15-3

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243977-15-3 Usage

Description

4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is an organic compound with the molecular formula C10H7F3N2. It is a derivative of quinoline, featuring an amino group at the 4th position and a trifluoromethyl group at the 8th position. 4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is known for its potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is used as an intermediate in the synthesis of various pharmaceutical compounds. Its presence in the molecular structure can contribute to the development of drugs with specific therapeutic properties.
Used in Rubber Industry:
In the rubber industry, 4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is used as a chemical additive to enhance the properties of rubber materials. It can improve the durability, flexibility, and resistance to various environmental factors, such as heat and UV radiation.
Used in Antimicrobial Applications:
4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is used as an antiseptic agent, helping to prevent the growth of harmful microorganisms and maintain cleanliness in various settings, such as medical facilities and personal care products.
Used in Antipyretic and Antiperiodic Applications:
4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is also utilized in the development of antipyretic drugs, which are designed to reduce fever and alleviate discomfort associated with high body temperature. Additionally, it is used in the synthesis of antiperiodic drugs, which are effective in treating conditions like malaria.
Used in Antimalarial Applications:
4-AMINO-8-(TRIFLUOROMETHYL)QUINOLINE is used as an antimalarial agent, playing a crucial role in the development of drugs that target and eliminate the Plasmodium parasite responsible for malaria. It is also used in the preparation of other antimalarial drugs, contributing to the global fight against this life-threatening disease.

Check Digit Verification of cas no

The CAS Registry Mumber 243977-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,3,9,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 243977-15:
(8*2)+(7*4)+(6*3)+(5*9)+(4*7)+(3*7)+(2*1)+(1*5)=163
163 % 10 = 3
So 243977-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H7F3N2/c11-10(12,13)7-3-1-2-6-8(14)4-5-15-9(6)7/h1-5H,(H2,14,15)

243977-15-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H50193)  4-Amino-8-(trifluoromethyl)quinoline, 97%   

  • 243977-15-3

  • 250mg

  • 546.0CNY

  • Detail
  • Alfa Aesar

  • (H50193)  4-Amino-8-(trifluoromethyl)quinoline, 97%   

  • 243977-15-3

  • 1g

  • 2184.0CNY

  • Detail

243977-15-3SDS

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 8-(trifluoromethyl)quinolin-4-amine

1.2 Other means of identification

Product number -
Other names 8-trifluoromethyl-quinolin-4-ylamine

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:243977-15-3 SDS

243977-15-3Downstream Products

243977-15-3Relevant articles and documents

In situ generation of ammonia for the copper-catalyzed synthesis of primary aminoquinolines

Aillerie, Alexandre,Pellegrini, Sylvain,Bousquet, Till,Pélinski, Lydie

, p. 1389 - 1391 (2014/05/06)

The synthesis of primary aminoquinolines from iodoquinolines was carried out in the presence of copper(i) iodide and formamide as the solvent and source of ammonia generated in situ. The reaction proceeded under mild conditions within a few hours and was applicable to various iodoquinolines.

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