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53871-27-5

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53871-27-5 Usage

General Description

1-(3-Fluorophenyl)pyrrole, 98% is a chemical compound that consists of a pyrrole ring with a fluorophenyl group attached to it. It is available in a high purity of 98%. Pyrrole compounds are commonly used in the synthesis of pharmaceuticals, agrochemicals, and materials for organic electronics. The presence of the fluorophenyl group in this compound may impart specific properties or reactivity that make it useful for certain applications. Overall, 1-(3-Fluorophenyl)pyrrole, 98% is a valuable building block for the production of various organic compounds with potential uses in a wide range of industries.

Check Digit Verification of cas no

The CAS Registry Mumber 53871-27-5 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 53871-27:
(7*5)+(6*3)+(5*8)+(4*7)+(3*1)+(2*2)+(1*7)=135
135 % 10 = 5
So 53871-27-5 is a valid CAS Registry Number.

53871-27-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H33348)  1-(3-Fluorophenyl)pyrrole, 98%   

  • 53871-27-5

  • 1g

  • 330.0CNY

  • Detail
  • Alfa Aesar

  • (H33348)  1-(3-Fluorophenyl)pyrrole, 98%   

  • 53871-27-5

  • 5g

  • 1098.0CNY

  • Detail
  • Alfa Aesar

  • (H33348)  1-(3-Fluorophenyl)pyrrole, 98%   

  • 53871-27-5

  • 25g

  • 3636.0CNY

  • Detail

53871-27-5SDS

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-fluorophenyl)-1H-pyrrole

1.2 Other means of identification

Product number -
Other names 1-(3-Fluorophenyl)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:53871-27-5 SDS

53871-27-5Downstream Products

53871-27-5Relevant articles and documents

The special directing effect of fluorine: Ligand independent ortho lithiation of 1-(fluorophenyl)pyrroles

Faigl, Ferenc,Fogassy, Katalin,Szanto, Zoltan,Lopata, Antal,Toeke, Laszlo

, p. 4367 - 4374 (1998)

Lithiation of l-(fluorophenyl)pyrroles occurred exclusively ortho to the fluorine substituent independently of the structure of the tertiary amine type ligands use. Semiempirical quantum chemical calculations confirmed that the special directing effect of

Pd-catalyzed nucleophilic fluorination of aryl bromides

Lee, Hong Geun,Milner, Phillip J.,Buchwald, Stephen L.

supporting information, p. 3792 - 3795 (2014/04/03)

On the basis of mechanism-driven reaction design, a Pd-catalyzed nucleophilic fluorination of aryl bromides and iodides has been developed. The method exhibits a broad substrate scope, especially with respect to nitrogen-containing heteroaryl bromides, and proceeds with minimal formation of the corresponding reduction products. A facilitated ligand modification process was shown to be critical to the success of the reaction.

Assisted tandem catalytic RCM-aromatization in the synthesis of pyrroles and furans

Schmidt, Bernd,Krehl, Stefan,Jablowski, Eric

, p. 5119 - 5130 (2012/08/07)

An assisted tandem catalytic transformation of diallyl amines and diallyl ethers into N-aryl pyrroles and furans, respectively, is described. The sequence relies on ring closing metathesis followed by dehydrogenation of the initially formed dihydropyrroles and dihydrofurans. Both steps are Ru-catalyzed, but the sequence requires only one precatalyst, because conversion of the metathesis catalyst into the dehydrogenation catalyst is achieved in situ, triggered by the oxidant tert-butyl hydroperoxide.

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