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N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is a chemical compound with the molecular formula C18H17NO3. It is an acetamide derivative featuring a benzyl group and a phenyl group attached to the nitrogen and carbon atoms, respectively. N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is widely utilized in organic synthesis and pharmaceutical research, and it holds potential for the development of new drugs in medicinal chemistry. The acetyl and benzyl groups in the molecule endow it with distinctive chemical and biological properties, making it a valuable asset for a range of research and industrial applications.

22426-99-9

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22426-99-9 Usage

Uses

Used in Organic Synthesis:
N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide array of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is used as a starting material or building block for the development of new drugs. Its chemical properties make it suitable for the creation of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Medicinal Chemistry:
N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is employed in medicinal chemistry for the design and optimization of drug candidates. Its unique structural features enable the exploration of new chemical space and the discovery of innovative therapeutic agents with improved efficacy and selectivity.
Used in Research and Development:
In the field of research and development, N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is utilized for studying the structure-activity relationships of biologically active compounds. Its presence in various chemical libraries aids researchers in identifying potential lead compounds and optimizing their properties for specific therapeutic targets.
Used in Industrial Applications:
N-ACETYL-N-(BENZYLOXY)-2-PHENYLACETAMIDE is also used in various industrial applications, such as the production of specialty chemicals, agrochemicals, and materials. Its unique chemical properties make it a valuable component in the development of innovative products and technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 22426-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22426-99:
(7*2)+(6*2)+(5*4)+(4*2)+(3*6)+(2*9)+(1*9)=99
99 % 10 = 9
So 22426-99-9 is a valid CAS Registry Number.

22426-99-9SDS

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 N-acetyl-2-phenyl-N-phenylmethoxyacetamide

1.2 Other means of identification

Product number -
Other names N-ethanoyl-2-phenyl-N-phenylmethoxy-ethanamide

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:22426-99-9 SDS

22426-99-9Relevant articles and documents

A NOVEL ELECTROPHILIC N-AMIDATION VIA ELECTRON DEFICIENT COMPLEXES : ACTION OF FERRIC CHLORIDE OF N-ACETYLOXYAMIDES

Cherest, Marc,Lusinchi, Xavier

, p. 715 - 718 (2007/10/02)

The action of FeCl3 on N-acetyloxyamides leads to electron deficient species which can react intra or intermolecularly with an aromatic group to give oxindoles or analogues.

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