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2-(4-chlorophenoxy)acetamide is a chemical compound with the molecular formula C8H8ClNO2. It is an amide derivative, characterized by the presence of an amide functional group (-CONH2) attached to a 2-(4-chlorophenoxy)acetic acid moiety. The compound features a 4-chlorophenoxy group, which is a chlorinated phenol ether, attached to the acetamide backbone. This chemical is known for its potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its ability to interact with biological systems. It is important to note that the handling and use of 2-(4-chlorophenoxy)acetamide should be done with caution, as it may have specific safety and environmental considerations.

3598-10-5

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3598-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3598-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3598-10:
(6*3)+(5*5)+(4*9)+(3*8)+(2*1)+(1*0)=105
105 % 10 = 5
So 3598-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO2/c9-6-1-3-7(4-2-6)12-5-8(10)11/h1-4H,5H2,(H2,10,11)

3598-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)acetamide

1.2 Other means of identification

Product number -
Other names 4-Chlorophenoxyacetamide

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:3598-10-5 SDS

3598-10-5Relevant academic research and scientific papers

PYRROLIDINE DERIVATIVES AS INHIBITOR OF FIBROBLAST ACTIVATION PROTEIN (FAP) AND PHARMACEUTICAL COMPOSITION INCLUDING THE SAME

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Paragraph 1826; 1830-1832, (2020/11/24)

The FAP inhibitor is represented by the following formula X. The present invention relates to a pyrrolidine derivative or a pharmaceutically acceptable salt thereof. Chem. X.

A phenoxy acetyl amine compound preparation method and phenoxy acetamide compounds

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Paragraph 0040; 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%.

Synthesis and biological evaluation of 2-Phenoxyacetamide analogues, a novel class of potent and selective monoamine oxidase inhibitors

Shen, Wei,Yu, Shian,Zhang, Jiaming,Jia, Weizheng,Zhu, Qing

, p. 18620 - 18631 (2015/01/08)

Monoamine oxidases (EC 1.4.3.4; MAOs), a family of FAD-containing enzymes, is an important target for antidepressant drugs. In this paper, a series of 2-phenoxyacetamide analogues were synthesized, and their inhibitory potency towards monoamine oxidases A (MAO-A) and B (MAO-B) were evaluated using enzyme and cancer cell lysate. 2-(4-Methoxyphenoxy)acetamide (compound 12) (SI = 245) and (2-(4-((prop-2- ynylimino)methyl)phenoxy)acetamide (compound 21) (IC50MAO-A = 0.018 μM, IC50MAO-B = 0.07 μM) were successfully identified as the most specific MAO-A inhibitor, and the most potent MAO-A/-B inhibitor, respectively. The inhibitory activities of these two compounds in living cells were also further evaluated utilizing HepG2 and SHSY-5Y cell lysates.

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