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35370-92-4

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35370-92-4 Usage

General Description

2-(4-Methoxyphenoxy)ethanethioamide is a chemical compound with the molecular formula C11H15NO2S. It is a thioamide derivative with a sulfurous functional group and a phenoxy group attached to a methyl group. 2-(4-METHOXYPHENOXY)ETHANETHIOAMIDE has potential applications in the field of pharmaceuticals, agrochemicals, and material science due to its unique chemical structure. It may be used as a building block in the synthesis of various organic compounds and may exhibit biological activity as well. However, further research is needed to fully understand the potential uses and properties of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 35370-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,7 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35370-92:
(7*3)+(6*5)+(5*3)+(4*7)+(3*0)+(2*9)+(1*2)=114
114 % 10 = 4
So 35370-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2S/c1-11-7-2-4-8(5-3-7)12-6-9(10)13/h2-5H,6H2,1H3,(H2,10,13)

35370-92-4 Well-known Company Product Price

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  • Alfa Aesar

  • (H26488)  2-(4-Methoxyphenoxy)thioacetamide, 97%   

  • 35370-92-4

  • 250mg

  • 240.0CNY

  • Detail
  • Alfa Aesar

  • (H26488)  2-(4-Methoxyphenoxy)thioacetamide, 97%   

  • 35370-92-4

  • 1g

  • 663.0CNY

  • Detail
  • Alfa Aesar

  • (H26488)  2-(4-Methoxyphenoxy)thioacetamide, 97%   

  • 35370-92-4

  • 5g

  • 2203.0CNY

  • Detail

35370-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-METHOXYPHENOXY)ETHANETHIOAMIDE

1.2 Other means of identification

Product number -
Other names 2-(4-Methoxyphenoxy)thioacetamide

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35370-92-4 SDS

35370-92-4Relevant articles and documents

Design, synthesis, biological evaluation and molecular modeling of N-isobutyl-N-((2-(p-tolyloxymethyl)thiazol-4yl)methyl)benzo[d][1,3] dioxole-5-carboxamides as selective butyrylcholinesterase inhibitors

Du, Chenxi,Du, Kui,Feng, Chengjie,Lv, Weiping,Shen, Runpu,Sun, Haopeng,Xi, Meiyang

supporting information, (2022/02/14)

Butyrylcholinesterase (BuChE) is recently regarded as a biomarker in progressed Alzheimer's disease (AD). Development of selective BuChE inhibitors has attracted a great deal of interest and may be a viable therapeutic strategy for AD. Recently, we reported the N-isobutyl-N-((2-(p-tolyloxymethyl)thiazol-4-yl)methyl)benzo[d][1,3]dioxole-5-carboxamide (1) as a selective BuChE inhibitor. Subsequently, 33 analogs were synthesized and assessed by AChE/BuChE activities, indicating an optimal compound 23. Further kinetic tests suggested a competitive manner. Molecular docking and Molecular dynamics (MD) simulation showed that it interacted with several residues in active site gorge of BuChE, possibly contributing to its selectivity and competitive pattern. Moreover, it showed low cytotoxicity and high blood brain barrier (BBB) permeability. Taken together, 23 was a promising BuChE inhibitor for the treatment of AD.

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