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1H-Pyrrole, 2-(trifluoromethyl)-, also known as a trifluoromethylated pyrrole, is a chemical compound characterized by the molecular formula C6H4F3N. It is a derivative of the heterocyclic aromatic organic compound pyrrole, with a trifluoromethyl group attached at the 2-position of the pyrrole ring. This modification endows the compound with unique chemical properties and reactivity, making it a versatile building block in various chemical and material sciences.

67095-60-7

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67095-60-7 Usage

Uses

Used in Pharmaceutical Research:
1H-Pyrrole, 2-(trifluoromethyl)is utilized as a key building block in the synthesis of pharmaceutical compounds. Its presence can enhance the bioactivity and pharmacokinetic properties of the resulting molecules, contributing to the development of new drugs with improved efficacy and safety profiles.
Used in Agrochemical Research:
In agrochemical applications, 1H-Pyrrole, 2-(trifluoromethyl)serves as a precursor for the creation of novel agrochemicals. Its incorporation into these compounds can lead to enhanced pesticidal properties, such as increased effectiveness against pests and resistance to environmental degradation.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1H-Pyrrole, 2-(trifluoromethyl)is employed for the introduction of the trifluoromethyl group into other organic compounds. This group is known to impart significant changes in the physical, chemical, and biological properties of molecules, which is valuable in the synthesis of new organic compounds with tailored characteristics.
Used in the Development of New Materials:
1H-Pyrrole, 2-(trifluoromethyl)has potential applications in the development of innovative materials. Its unique properties can be leveraged to create materials with specific functionalities, such as improved thermal stability, chemical resistance, or electronic properties, which are crucial in various industries.
Used as a Ligand in Coordination Chemistry:
In coordination chemistry, 1H-Pyrrole, 2-(trifluoromethyl)can act as a ligand, forming complexes with metal ions. These complexes can exhibit novel properties and reactivities, which are of interest in catalysis, sensing, and other areas of chemical research and application.
Overall, 1H-Pyrrole, 2-(trifluoromethyl)is a multifaceted compound with applications spanning across medicine, agriculture, materials science, and beyond, reflecting its importance in the advancement of these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 67095-60-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,9 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67095-60:
(7*6)+(6*7)+(5*0)+(4*9)+(3*5)+(2*6)+(1*0)=147
147 % 10 = 7
So 67095-60-7 is a valid CAS Registry Number.

67095-60-7SDS

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 2-(trifluoromethyl)-1H-pyrrole

1.2 Other means of identification

Product number -
Other names 2-trifluoromethylpyrrole

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:67095-60-7 SDS

67095-60-7Downstream Products

67095-60-7Relevant academic research and scientific papers

TRIFLUORMETHYLIERUNGSREAKTIONEN VON CF3I, Te(CF3)2, Sb(CF3)3, Hg(CF3)2, UND Cd(CF3)2*D MIT FURAN, THIOPHEN, PYRROL UND p-BENZOCHINON

Naumann, Dieter,Kischkewitz, Juergen

, p. 265 - 281 (2007/10/02)

The trifluoromethylation reactions of Cd(CF3)2*glyme, Hg(CF3)2, Sb(CF3)3, CF3I, and Te(CF3)2 with furan, thiophene, pyrrol, and p-benzoquinone are compared under similar conditions.During the photochemical reactions the reactivity increases in the series

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