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215649-72-2

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215649-72-2 Usage

Derivative of acetamide

It is a modified version of the simple organic compound acetamide, which has a similar structure.

Contains a trifluoromethoxyphenyl group

The chemical has a phenyl ring with a trifluoromethoxy substituent, which is a group consisting of a carbon atom bonded to three fluorine atoms and an ether oxygen atom.

Potential drug candidate

Due to its pharmacological properties, this chemical may have potential applications in the development of new drugs.

Pharmacological properties

The specific pharmacological properties are not mentioned in the material provided, but they contribute to its potential as a drug candidate.

Applications in the pharmaceutical industry

The chemical may be useful in the development of medications for various medical conditions.

Potential to be harmful

It is important to handle this chemical with care, as it may cause harm if not used or stored properly.

Promising properties

The chemical has properties that make it of interest in various fields, although the specific fields are not mentioned in the material provided.

Check Digit Verification of cas no

The CAS Registry Mumber 215649-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,6,4 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 215649-72:
(8*2)+(7*1)+(6*5)+(5*6)+(4*4)+(3*9)+(2*7)+(1*2)=142
142 % 10 = 2
So 215649-72-2 is a valid CAS Registry Number.

215649-72-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethylamino)-N-[3-(trifluoromethoxy)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names -

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:215649-72-2 SDS

215649-72-2Downstream Products

215649-72-2Relevant articles and documents

Efficient synthesis of N-arylpiperazinones via a selective intramolecular Mitsunobu cyclodehydration

Weissman, Steven A.,Lewis, Stephanie,Askin, David,Volante,Reider, Paul J.

, p. 7459 - 7462 (2007/10/03)

A practical two pot synthesis of N-arylpiperazinones from the corresponding aniline is described. The key transformation is a selective intramolecular Mitsunobu cyclodehydration of an amidoalcohol intermediate. A series of N-arylpiperazinones were prepared in yields up to 89%.

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