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ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE is a pyrimidine derivative chemical compound characterized by its molecular formula C9H6F6N2O2. It features two trifluoromethyl groups at the 2 and 4 positions of the pyrimidine ring and an ethyl ester group at the 5 position, presenting a white solid form with a molecular weight of 278.15 g/mol. ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE is recognized for its unique chemical structure and reactivity, making it a valuable building block in the synthesis of pharmaceutical and agrochemical compounds.

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  • 5-Pyrimidinecarboxylicacid, 2,4-bis(trifluoromethyl)-, ethyl ester Manufacturer/High quality/Best price/In stock

    Cas No: 188781-15-9

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  • BEST PRICE/5-Pyrimidinecarboxylicacid, 2,4-bis(trifluoromethyl)-, ethyl ester CAS NO.188781-15-9

    Cas No: 188781-15-9

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  • 188781-15-9 Structure
  • Basic information

    1. Product Name: ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE
    2. Synonyms: ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE;2,4-BIS-(TRIFLUOROMETHYL)PYRIMIDINE-5-CARBOXYLIC ACID ETHYL ESTER
    3. CAS NO:188781-15-9
    4. Molecular Formula: C9H6F6N2O2
    5. Molecular Weight: 288.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 188781-15-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 227.1°Cat760mmHg
    3. Flash Point: 91.2°C
    4. Appearance: /
    5. Density: 1.46g/cm3
    6. Vapor Pressure: 0.079mmHg at 25°C
    7. Refractive Index: 1.409
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE(188781-15-9)
    12. EPA Substance Registry System: ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE(188781-15-9)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 188781-15-9(Hazardous Substances Data)

188781-15-9 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE serves as a building block for the creation of novel agrochemicals. Its incorporation into these compounds can lead to enhanced crop protection and management solutions.
Used in Medicinal Chemistry Research:
ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE is utilized in medicinal chemistry research for exploring its potential biological activities. Studies on this compound may reveal new avenues for drug discovery and the development of treatments for various diseases.
Used in Agricultural Research:
ETHYL-2-TRIFLUOROMETHYL-4-TRIFLUOROMETHYL-5-PYRIMIDINE CARBOXYLATE is also studied in agricultural research to understand its possible applications in enhancing crop yields, improving resistance to pests and diseases, and developing more effective and environmentally friendly agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 188781-15-9 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188781-15:
(8*1)+(7*8)+(6*8)+(5*7)+(4*8)+(3*1)+(2*1)+(1*5)=189
189 % 10 = 9
So 188781-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F6N2O2/c1-2-19-6(18)4-3-16-7(9(13,14)15)17-5(4)8(10,11)12/h3H,2H2,1H3

188781-15-9SDS

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 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 2,4-bis(trifluoromethyl)pyrimidine-5-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:188781-15-9 SDS

188781-15-9Relevant 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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