Welcome to LookChem.com Sign In|Join Free
  • or
N-3-quinolylacetamide is an organic compound with the chemical formula C12H10N2O. It is a derivative of quinoline, a heterocyclic aromatic compound, and acetamide, an amide of acetic acid. N-3-quinolylacetamide is characterized by a quinoline ring fused to a pyridine ring, with an acetamide group attached to the 3-position of the quinoline. N-3-quinolylacetamide is a white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and agrochemicals. It is also known for its potential biological activities, including antimicrobial and anticancer properties, although further research is needed to fully understand its therapeutic potential.

5417-50-5

Post Buying Request

5417-50-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5417-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5417-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5417-50:
(6*5)+(5*4)+(4*1)+(3*7)+(2*5)+(1*0)=85
85 % 10 = 5
So 5417-50-5 is a valid CAS Registry Number.

5417-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-quinolin-3-ylacetamide

1.2 Other means of identification

Product number -
Other names 3-Acetylamino-chinolin

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:5417-50-5 SDS

5417-50-5Relevant academic research and scientific papers

Enantioselective transfer hydrogenation, a key step for the synthesis of 3-aminotetrahydroquinolines

Aillerie, Alexandre,Lemau De Talencé, Vincent,Dumont, Clément,Pellegrini, Sylvain,Capet, Frédéric,Bousquet, Till,Pélinski, Lydie

, p. 9034 - 9037 (2016)

An enantioselective transfer hydrogenation has been successfully achieved to furnish 3-aminotetrahydroquinolines. The reaction was conducted in the presence of Hantzsch dihydropyridine and a catalytic amount of chiral phosphoric acid under mild conditions.

Wasalexins A and B, new phytoalexins from wasabi: Isolation, synthesis, and antifungal activity

Pedras, M. Soledade C.,Sorensen, John L.,Okanga, Francis I.,Zaharia, Irina L.

, p. 3015 - 3020 (1999)

The chemical structure determination of two phytoalexins from wasabi (Wasabia japonica, syn. Eutrema wasabi), a plant resistant to virulent isolates of the blackleg fungus [Leptosphaeria maculans (Desm.) Ces. et de Not., asexual stage Phoma lingam (Tode ex Fr.) Desm.], as well as their synthesis and antifungal activity towards isolates of P. lingam and P. wasabiae is reported.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5417-50-5