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3'-METHYLPHENOXYACETAMIDE is a chemical compound derived from acetamide, featuring a methyl group at the 3' position on a phenyl ring and a phenoxy group attached to the acetamide functional group. It serves as a versatile building block in organic synthesis and pharmaceutical research, with potential applications in drug development due to its unique structural features and possible biological activities.

10017-53-5

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10017-53-5 Usage

Uses

Used in Organic Synthesis:
3'-METHYLPHENOXYACETAMIDE is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3'-METHYLPHENOXYACETAMIDE is used as a precursor in the development of new drugs and pharmaceuticals. Its structural features and potential biological activities make it a promising candidate for further research and exploration.
However, it is important to note that further research is required to fully understand the properties and potential uses of 3'-METHYLPHENOXYACETAMIDE in the pharmaceutical industry, ensuring its safety and efficacy in drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 10017-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,1 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10017-53:
(7*1)+(6*0)+(5*0)+(4*1)+(3*7)+(2*5)+(1*3)=45
45 % 10 = 5
So 10017-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-7-3-2-4-8(5-7)12-6-9(10)11/h2-5H,6H2,1H3,(H2,10,11)

10017-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-Methylphenoxyacetamide

1.2 Other means of identification

Product number -
Other names 2-(3-methylphenoxy)acetamide

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:10017-53-5 SDS

10017-53-5Relevant academic research and scientific papers

A phenoxy acetyl amine compound preparation method and phenoxy acetamide compounds

-

Paragraph 0040; 0042; 0047; 0048; 0049-0053, (2019/05/21)

The invention belongs to the organic intermediates and the technical field of pharmaceutical intermediates, in particular to a phenoxy acetyl amine compound preparation method and phenoxy acetyl amine compound. The present invention provides a preparation method of the pervasive should be good, and green environmental protection, has better popularization and application value. The results show that the embodiment, the invention provides the above-mentioned method can prepare a plurality of phenoxy acetyl amine compound, and the yield can be 76%.

The synthesis of ethacrynic acid thiazole derivatives as glutathione S-transferase pi inhibitors

Li, Ting,Liu, Guyue,Li, Hongcai,Yang, Xinmei,Jing, Yongkui,Zhao, Guisen

, p. 2316 - 2322 (2012/05/07)

Glutathione S-transferase pi (GSTpi) is a phase II enzyme which protects cells from death and detoxifies chemotherapeutic agents in cancer cells. Ethacrynic acid (EA) is a weak GSTpi inhibitor. Structure modifications were done to improve the ability of EA to inhibit GSTpi activity. Eighteen EA thiazole derivatives were designed and synthesized. Compounds 9a, 9b and 9c with a replacement of carboxyl group of EA by a heterocyclic thiazole exhibited improvement over EA to inhibit GSTpi activity.

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