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55403-91-3

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55403-91-3 Usage

General Description

1-(2-chloro-4-nitrophenyl)pyrrolidine is a chemical compound that belongs to the pyrrolidine family. It is a substituted pyrrolidine derivative with a chloro and a nitro group on the phenyl ring. The chemical formula of 1-(2-chloro-4-nitrophenyl)pyrrolidine is C10H10ClN2O2, and its molecular weight is 232.65 g/mol. 1-(2-chloro-4-nitrophenyl)pyrrolidine may have potential applications in pharmaceutical and industrial fields, and it is important to handle it with care due to its potential health hazards such as skin irritation and environmental impact. More research and testing may be needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 55403-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,0 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55403-91:
(7*5)+(6*5)+(5*4)+(4*0)+(3*3)+(2*9)+(1*1)=113
113 % 10 = 3
So 55403-91-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClN2O2/c11-9-7-8(13(14)15)3-4-10(9)12-5-1-2-6-12/h3-4,7H,1-2,5-6H2

55403-91-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H63415)  1-(2-Chloro-4-nitrophenyl)pyrrolidine, 97%   

  • 55403-91-3

  • 250mg

  • 245.0CNY

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  • Alfa Aesar

  • (H63415)  1-(2-Chloro-4-nitrophenyl)pyrrolidine, 97%   

  • 55403-91-3

  • 1g

  • 735.0CNY

  • Detail
  • Alfa Aesar

  • (H63415)  1-(2-Chloro-4-nitrophenyl)pyrrolidine, 97%   

  • 55403-91-3

  • 5g

  • 2940.0CNY

  • Detail

55403-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Chloro-4-nitro-phenyl)-pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-chloro-1-pyrrolidino-4-nitrobenzene

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

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More Details:55403-91-3 SDS

55403-91-3Relevant articles and documents

Cobalt-catalyzed C-N bond-forming reaction between chloronitrobenzenes and secondary amines

Toma, Gabriel,Yamaguchi, Ryohei

experimental part, p. 6404 - 6408 (2011/02/22)

Cyclic secondary amines react with mono- or dichloronitrobenzene in the presence of a catalytic amount of cobalt(II) chloride. Phosphane ligands are beneficial for the reaction, although the bite-angle effect was not strong. The nitro-substituted tertiary amines formed are important as bioactive compounds and can also be intermediates for the synthesis of substituted anilines. This work represents the first cobalt-catalyzed approach to C-N bond-forming reactions involving aromatic chlorides and cyclic secondary amines. The reaction is ortho- and para-selective, with meta-substituted halides being unreactive in this procedure. The first cobalt-catalyzed C-N bond-forming reaction involving aromatic chlorides and cyclic secondary amines is described.The reaction is ortho- and para-selective; meta-substituted halides are unreactive. Copyright

Aromatic Nucleophilic Substitution of Halobenzenes with Amines under High Pressure

Ibata, Toshikazu,Isogami, Yasushi,Toyoda, Jiro

, p. 42 - 49 (2007/10/02)

The nucleophilic substitution reactions of aromatic halides having electron-attracting groups on ortho or para position with various primary and secondary amines were accelerated by high pressure to give the corresponding N-substituted anilines in high yields.The bulkiness of amines affects its reactivity to lower the yields of the products.Although the secondary amines are usually less reactive than primary amines, cyclic secondary amines such as morpholine, piperidine, and pyrrolidine were found very reactive. 1,4-Diazabicyclooctane and quinuclidine gave N-quarternary ammonium halides in high yields in contrast to the low reactivity of acyclic tertiary amines.Dichloro- and trichloro-nitrobenzenes also react with diethylamine, pyrrolidine, and morpholine to give mono-, di-, and trisubstitution products depending upon the amount of amine and the position of nitro group in these chlorides.

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