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1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE is a chemical compound that belongs to the group of organofluorine compounds, which are organic compounds that consist of a carbon-fluorine bond. It features a trifluoromethoxy group (an ether with a trifluoromethyl group attached to the oxygen atom), a phenyl group, and a pyrrole-2,5-dione group. The properties and potential uses of 1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE are influenced by these functional groups. However, its specific applications are not extensively documented in the literature, suggesting that it may not be a widely studied or utilized compound.

68255-58-3

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68255-58-3 Usage

Uses

Since the specific applications of 1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE are not readily found in the literature, it is difficult to list its uses in various industries. However, given its classification as an organofluorine compound and the presence of its functional groups, it can be inferred that it may have potential applications in the following areas:
Used in Pharmaceutical Industry:
1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE could be used as a building block or intermediate in the synthesis of pharmaceutical compounds, given the presence of the phenyl and pyrrole-2,5-dione groups, which are common in many drug molecules.
Used in Chemical Research:
1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE may serve as a subject of study in chemical research, particularly in the field of organofluorine chemistry, to explore its reactivity, stability, and potential applications in the synthesis of other compounds.
Used in Material Science:
The trifluoromethoxy group and the phenyl group in 1-[4-(TRIFLUOROMETHOXY)PHENYL]-1H-PYRROLE-2,5-DIONE could potentially contribute to unique material properties, making it a candidate for investigation in material science for possible applications in the development of new materials with specific characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 68255-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 68255-58:
(7*6)+(6*8)+(5*2)+(4*5)+(3*5)+(2*5)+(1*8)=153
153 % 10 = 3
So 68255-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H6F3NO3/c12-11(13,14)18-8-3-1-7(2-4-8)15-9(16)5-6-10(15)17/h1-6H

68255-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-(trifluoromethoxy)phenyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-[4-(trifluoromethoxy)phenyl]azoline-2,5-dione

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:68255-58-3 SDS

68255-58-3Relevant academic research and scientific papers

Photochemical Reaction of N,N-Dimethylanilines with N-Substituted Maleimides Utilizing Benzaldehyde as the Photoinitiator

Nikitas, Nikolaos F.,Theodoropoulou, Maria A.,Kokotos, Christoforos G.

supporting information, p. 1168 - 1173 (2021/02/01)

Photoorganocatalysis constitutes a powerful domain of photochemistry and organic synthesis. The scaffold of pyrrolo[3,4-c]quinolinoles exhibits interesting and potent inhibition against various enzymes, making them really promising pharmaceutical targets. Herein, we describe a photochemical methodology for the reaction of N,N-dimethylanilines with N-substituted maleimides, utilizing benzaldehyde as the photoinitiator. A variety of substituted N,N-dimethylanilines and N-substituted maleimides were converted into the corresponding adducts in moderate to high yields.

Preparation method for fluorinated maleimide derivative and application of fluorinated maleimide derivative

-

Paragraph 0031-0037; 0039-0050, (2019/02/13)

The invention discloses a preparation method for a fluorinated maleimide derivative and an application of the fluorinated maleimide derivative and belongs to the technical field of organic synthesis.The preparation method for the fluorinated maleimide der

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