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35368-44-6

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35368-44-6 Usage

General Description

2-(4-Chlorophenoxy)thioacetamide is a chemical compound with the molecular formula C8H8ClNOS. It is a thioamide derivative, in which a thioacetamide group is attached to a 4-chlorophenoxy group. 2-(4-CHLOROPHENOXY)THIOACETAMIDE may have potential applications in the fields of pharmaceuticals and agriculture due to its structural features and potential biological activities. However, further research is required to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 35368-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,6 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35368-44:
(7*3)+(6*5)+(5*3)+(4*6)+(3*8)+(2*4)+(1*4)=126
126 % 10 = 6
So 35368-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNOS/c9-6-1-3-7(4-2-6)11-5-8(10)12/h1-4H,5H2,(H2,10,12)

35368-44-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L12711)  2-(4-Chlorophenoxy)thioacetamide, 97%   

  • 35368-44-6

  • 1g

  • 428.0CNY

  • Detail
  • Alfa Aesar

  • (L12711)  2-(4-Chlorophenoxy)thioacetamide, 97%   

  • 35368-44-6

  • 5g

  • 1629.0CNY

  • Detail

35368-44-6SDS

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-chlorophenoxy)ethanethioamide

1.2 Other means of identification

Product number -
Other names (4-Chlor-phenoxy)-thioessigsaeure-amid

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:35368-44-6 SDS

35368-44-6Relevant articles and documents

Synthesis and Antitubercular Activity of 4-(5-Nitro-2-furyl/2-pyrazinyl/1-adamantyl)-2-(alkyl/aryl/arylamino)thiazoles

Khadse, B. G.,Lokhande, S. R.,Bhamaria, R. P.,Prabhu, S. R.

, p. 856 - 860 (2007/10/02)

The reaction of haloketones, obtained from Arndt-Eistert reaction on the acid chlorides of 1-adamantane, 5-nitrofuroic acid and pyrazine-2-carboxylic acid, with different thioamides and thioureas affords the title thiazoles (I-III).Some of them exhibit interesting antitubercular activity at 6.25 to 0.38 μg/ml concentration against H37Rv strain of M. tubercolosis in vitro testing.The structure activity relationship (SAR) has also been discussed.

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