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2-(4-nitrophenyl)-2-oxoethyl piperidine-1-carbodithioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24372-63-2

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24372-63-2 Usage

Chemical class

Piperidine derivatives

Structure

Piperidine ring with a carbodithioate group attached to the nitrogen atom, and a 2-(4-nitrophenyl)-2-oxoethyl moiety

Potential applications

Pharmaceutical research and drug discovery, specifically in the development of new medications with anti-inflammatory, antibacterial, or antifungal properties

Use as a reagent

Chemical synthesis and organic reactions, due to its unique chemical structure and properties

Safety precautions

Handle with care and follow proper safety protocols to minimize potential health and environmental risks if not used and disposed of properly.

Check Digit Verification of cas no

The CAS Registry Mumber 24372-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24372-63:
(7*2)+(6*4)+(5*3)+(4*7)+(3*2)+(2*6)+(1*3)=102
102 % 10 = 2
So 24372-63-2 is a valid CAS Registry Number.

24372-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-nitrophenyl)-2-oxoethyl] piperidine-1-carbodithioate

1.2 Other means of identification

Product number -
Other names 2-(4-nitrophenyl)-2-oxoethyl tetrahydro-1(2H)-pyridinecarbodithioate

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:24372-63-2 SDS

24372-63-2Downstream Products

24372-63-2Relevant academic research and scientific papers

A novel isocyanide-based three-component reaction: A facile synthesis of substituted 2H-pyran-3,4-dicarboxylates

Khalilzadeh, Mohammad A.,Hossaini, Zinatossadat,Baradarani, Mohammad M.,Hasannia, Adel

experimental part, p. 8464 - 8467 (2010/11/19)

An efficient method for synthesis of 2H-pyran-3,4-dicarboxylates using the three-component reaction of dithiocarbamates, dialkyl acetylenedicarboxylates, and isocyanides in solvent-free conditions is described. In these reactions, synthesis of dithiocarbamates is possibly based on the one-pot reaction of secondary amines, CS2, and alkyl halides in solvent-free conditions without using a catalyst. The mild reaction conditions and high yields of the reaction exhibit the good synthetic advantage of these methods.

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