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619-56-7

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619-56-7 Usage

Chemical Properties

WHITE FINE CRYSTALLINE POWDER

Synthesis Reference(s)

Synthetic Communications, 20, p. 563, 1990 DOI: 10.1080/00397919008244905Synthesis, p. 243, 1980

Check Digit Verification of cas no

The CAS Registry Mumber 619-56-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 619-56:
(5*6)+(4*1)+(3*9)+(2*5)+(1*6)=77
77 % 10 = 7
So 619-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H6ClNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)

619-56-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A13809)  4-Chlorobenzamide, 98+%   

  • 619-56-7

  • 10g

  • 448.0CNY

  • Detail
  • Alfa Aesar

  • (A13809)  4-Chlorobenzamide, 98+%   

  • 619-56-7

  • 50g

  • 1807.0CNY

  • Detail
  • Alfa Aesar

  • (A13809)  4-Chlorobenzamide, 98+%   

  • 619-56-7

  • 250g

  • 7698.0CNY

  • Detail

619-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chlorobenzamide

1.2 Other means of identification

Product number -
Other names p-chlorophenylcarboxamide

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:619-56-7 SDS

619-56-7Relevant articles and documents

Advantage of anaerobic conditions in the highly enantioselective synthesis of α,α-dialkyl-α-amino acids by chiral phase-transfer catalysis

Ooi,Takeuchi,Ohara,Maruoka

, p. 1185 - 1187 (2001)

Intervention of the enolate oxidation in the catalytic asymmetric phase-transfer alkylation of protected α-amino acid derivatives under aerobic conditions has been addressed, and anaerobic conditions have been introduced to obtain synthetically satisfactory chemical yields as well as a high level of enantioselectivity.

Design of gp120 HIV-1 entry inhibitors by scaffold hopping via isosteric replacements

Ahmed, Shahad,Altieri, Andrea,Belov, Dmitry S.,Curreli, Francesca,Debnath, Asim K.,Iusupov, Ildar R.,Kurkin, Alexander V.,Manasova, Ekaterina V.,Markov, Pavel O.,Spiridonov, Evgeniy A.

, (2021/07/13)

We present the development of alternative scaffolds and validation of their synthetic pathways as a tool for the exploration of new HIV gp120 inhibitors based on the recently discovered inhibitor of this class, NBD-14136. The new synthetic routes were based on isosteric replacements of the amine and acid precursors required for the synthesis of NBD-14136, guided by molecular modeling and chemical feasibility analysis. To ensure that these synthetic tools and new scaffolds had the potential for further exploration, we eventually tested few representative compounds from each newly designed scaffold against the gp120 inhibition assay and cell viability assays.

CuO-decorated magnetite-reduced graphene oxide: a robust and promising heterogeneous catalyst for the oxidative amidation of methylarenes in waterviabenzylic sp3C-H activation

Ebrahimi, Edris,Khalafi-Nezhad, Ali,Khalili, Dariush,Rousta, Marzieh

, p. 20007 - 20020 (2021/11/12)

A magnetite-reduced graphene oxide-supported CuO nanocomposite (rGO/Fe3O4-CuO) was preparedviaa facile chemical method and characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), UV-vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS), Brunauer-Emmett-Teller (BET) analysis, vibrating-sample magnetometry (VSM), and thermogravimetric (TG) analysis. The catalytic activity of the rGO/Fe3O4-CuO nanocomposite was probed in the direct oxidative amidation reaction of methylarenes with free amines. Various aromatic and aliphatic amides were prepared efficiently at room temperature from cheap raw chemicals usingtert-butyl hydroperoxide (TBHP) as a “green” oxidant and low-toxicity TBAI in water. This method combines the oxidation of methylarenes and amide bond formation into a single operation. Moreover, the synthesized nanocomposites can be separated from the reaction mixtures using an external magnet and reused in six consecutive runs without a noticeable decrease in the catalytic activity.

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