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4-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylic acid is a complex organic compound with the molecular formula C12H8F3N3O2. It features a pyrimidine core, which is a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound is characterized by the presence of a trifluoromethyl group (-CF3) attached to a phenyl ring, which is further connected to the pyrimidine core through an amino group. The carboxylic acid functional group (-COOH) is located at the 5-position of the pyrimidine ring, providing the molecule with acidic properties. This chemical structure may be relevant in the context of pharmaceuticals or materials science, potentially serving as a building block for the development of new drugs or other chemical products.

6454-66-6

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6454-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6454-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6454-66:
(6*6)+(5*4)+(4*5)+(3*4)+(2*6)+(1*6)=106
106 % 10 = 6
So 6454-66-6 is a valid CAS Registry Number.

6454-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[3-(trifluoromethyl)anilino]pyrimidine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-(3-Trifluoromethylanilino)pyrimidine-5-carboxylic acid

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:6454-66-6 SDS

6454-66-6Downstream Products

6454-66-6Relevant academic research and scientific papers

Synthetic studies on novel Syk inhibitors. Part 1: Synthesis and structure-activity relationships of pyrimidine-5-carboxamide derivatives

Hisamichi, Hiroyuki,Naito, Ryo,Toyoshima, Akira,Kawano, Noriyuki,Ichikawa, Atsushi,Orita, Akiko,Orita, Masaya,Hamada, Noritaka,Takeuchi, Makoto,Ohta, Mitsuaki,Tsukamoto, Shin-Ichi

, p. 4936 - 4951 (2007/10/03)

Spleen tyrosine kinase (Syk) is a non-receptor-type tyrosine kinase which mediates diverse responses in haematopoietic cells. Therefore, Syk is an attractive therapeutic target, and in a study of Syk inhibitors as potentially new therapeutic agents, we di

Heterocyclen-Synthesen mit Monothiomalonsaeure-Amiden: Synthese von 3-Oxo-2,3-dihydroisothiazolopyridinen und 3-Oxo-2,3-dihydroisothiazolopyrimidinen

Schaper, Wolfgang

, p. 861 - 867 (2007/10/02)

The monothiomalonic acid amides 5, prepared from cyanoacetamides 4 and hydrogen sulphide, react with diketones 6 or aldehyde derivatives 7 to give the 2-thioxo-1,2-dihydropyridine-3-carboxamides 8 which can be cyclised to the 3-oxo-2,3-dihydroisothiazolo

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