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53871-26-4

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53871-26-4 Usage

Purity

98%

Type of Compound

Pyrrole derivative

Structural Features

Five-membered aromatic heterocyclic ring
Trifluoromethylphenyl substituent

Trifluoromethylphenyl Group

Benzene ring with a trifluoromethyl substituent

Applications

Pharmaceutical industry
Agrochemical industry

Usage

Synthesis of various organic compounds

Potential

Building block in the development of new drugs and pesticides

Suitability

Research and development activities in the chemical and pharmaceutical industries

Unique Structural Properties

Contributes to its potential in drug and pesticide development

Check Digit Verification of cas no

The CAS Registry Mumber 53871-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,7 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53871-26:
(7*5)+(6*3)+(5*8)+(4*7)+(3*1)+(2*2)+(1*6)=134
134 % 10 = 4
So 53871-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H8F3N/c12-11(13,14)9-4-3-5-10(8-9)15-6-1-2-7-15/h1-8H

53871-26-4 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H33444)  1-[3-(Trifluoromethyl)phenyl]pyrrole, 98%   

  • 53871-26-4

  • 1g

  • 487.0CNY

  • Detail
  • Alfa Aesar

  • (H33444)  1-[3-(Trifluoromethyl)phenyl]pyrrole, 98%   

  • 53871-26-4

  • 5g

  • 1629.0CNY

  • Detail
  • Alfa Aesar

  • (H33444)  1-[3-(Trifluoromethyl)phenyl]pyrrole, 98%   

  • 53871-26-4

  • 25g

  • 5415.0CNY

  • Detail

53871-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(trifluoromethyl)phenyl]pyrrole

1.2 Other means of identification

Product number -
Other names 1-[3-(trifluoromethyl)phenyl]-1H-pyrrole

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:53871-26-4 SDS

53871-26-4Downstream Products

53871-26-4Relevant articles and documents

Lactam derivatives and preparation method and application thereof

-

Paragraph 0048-0052; 0076; 0079, (2020/02/10)

The invention relates to lactam derivatives and a preparation method and application thereof. Compared with the prior art, the invention provides lactam compounds with a novel structure. The compoundsand compositions thereof have remarkable activity in inhibition of the proliferation of cancer cells (including, but not limited to, the liver cancer cell line HepG2 and the lung cancer cell line A549), and the activity of multiple compounds is in the same order of magnitude as the activity of the commercial drug adriamycin or superior to the activity of adriamycin. The compounds of the inventioncan be prepared from N-substituted pyrrole compounds through a reaction, and the preparation method is convenient, rapid and efficient.

L-(+)-Tartaric acid and choline chloride based deep eutectic solvent: An efficient and reusable medium for synthesis of N-substituted pyrroles via Clauson-Kaas reaction

Wang, Ping,Ma, Fei-Ping,Zhang, Zhan-Hui

, p. 259 - 262 (2014/11/07)

l-(+)-Tartaric acid-choline chloride based deep eutectic solvent has been found to be an effective promoted medium for Clauson-Kaas reaction of aromatic amines and 2,5-dimethoxytetrahydrofuran. Structurally diverse N-substituted pyrroles were obtained in high to excellent yields under mild conditions. The deep eutectic solvent is inexpensive, non-toxic, reusable and biodegradable.

Unique chemoselective Clauson-Kass reaction of substituted aniline catalyzed by MgI2 etherate

Zhang, Xingxian,Shi, Junchen

experimental part, p. 898 - 903 (2011/03/19)

Clauson-Kass reaction of various substituted aniline, primary aryl amide, and sufonyl amide with 2,5-dimethoxytetrahydrofuran was realized in the presence of 10 mol % of MgI2 etherate in a mild, efficient, and highly chemoselective manner. Iodide counterion and solvents (i.e., MeCN) played the critical roles for the unique reactivity of this catalytic system.

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