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2,4-BIS(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID, also known as BTCPA, is a pyrimidine carboxylic acid derivative with a distinctive molecular structure featuring a pyrimidine ring substituted with two trifluoromethyl groups at the 2 and 4 positions and a carboxylic acid group at the 5 position. This chemical compound is recognized for its unique chemical properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agricultural chemicals, as well as a potent pharmacophore for drug design and development.

188781-46-6

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188781-46-6 Usage

Uses

Used in Pharmaceutical Industry:
2,4-BIS(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical properties and its role as a potent pharmacophore, which aids in the development of new drugs with improved therapeutic effects.
Used in Agricultural Chemical Industry:
In the agricultural chemical industry, 2,4-BIS(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID is utilized as a key intermediate in the production of a range of agrochemicals, contributing to the development of effective pest control agents and other agricultural products.
Used in Organic Compounds Synthesis:
2,4-BIS(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID is employed as a valuable intermediate in the synthesis of a wide array of organic compounds for industrial applications, leveraging its electron-withdrawing trifluoromethyl groups and carboxylic acid functionality to enhance the properties of the resulting compounds.
Used in Research and Development:
2,4-BIS(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID is also used as a research tool in academic and industrial research settings, where its unique structure and properties are explored for potential applications in new drug discovery and the development of innovative materials.

Check Digit Verification of cas no

The CAS Registry Mumber 188781-46-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 188781-46:
(8*1)+(7*8)+(6*8)+(5*7)+(4*8)+(3*1)+(2*4)+(1*6)=196
196 % 10 = 6
So 188781-46-6 is a valid CAS Registry Number.

188781-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,4-bis (trifluoromethyl)-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:188781-46-6 SDS

188781-46-6Downstream Products

188781-46-6Relevant articles and documents

Inhibitors of NF-kappaB and AP-1 gene expression: SAR studies on the pyrimidine portion of 2-chloro-4-trifluoromethylpyrimidine-5-[N-(3', 5'-bis(trifluoromethyl)phenyl)carboxamide].

Palanki,Erdman,Gayo-Fung,Shevlin,Sullivan,Goldman,Ransone,Bennett,Manning,Suto

, p. 3995 - 4004 (2007/10/03)

We investigated the structure-activity relationship studies of N-[3, 5-bis(trifluoromethyl)phenyl][2-chloro-4-(trifluoromethyl)pyrimidin-5 -yl]carboxamide (1), an inhibitor of transcription mediated by both NF-kappaB and AP-1 transcription factors, with the goal of improving its potential oral bioavailability. Compounds were examined for cell-based activity, were fit to Lipinski's rule of 5, and were examined for potential gastrointestinal permeability using the intestinal epithelial cell line, Caco-2. Selected groups were substituted at the 2-, 4-, and 5-positions of the pyrimidine ring using solution-phase combinatorial methodology. The introduction of a fluorine in the place of 2-chlorine of 1 resulted in a compound with comparable activity. However, other substitutions at the 2-position resulted in a loss of activity. The trifluoromethyl group at the 4-position could be replaced with a methyl, ethyl, chlorine, or phenyl without a substantial loss of activity. The carboxamide group at the 5-position is critical for activity. If it was moved to the 6-position, the activity was lost. The 2-methyl analogue of 1 (81) showed comparable in vitro activity and improved Caco-2 permeability compared to 1.

Pyrimidine carboxamides and related compounds and methods for treating inflammatory conditions

-

, (2008/06/13)

Compounds having utility as antinflammatory agents in general and, more specifically, for the prevention and/or treatment of immunoinflammatory and autoimmune diseases are disclosed. The compounds are pyrimidine- or pyrazine-containing compounds and, in one embodiment, are carboxyamides of the same. Methods are also disclosed for preventing and/or treating inflammatory conditions by administering to an animal in need thereof an effective amount of a compound of this invention, preferably in the form of a pharmaceutical composition.

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