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N-[4-[4-[4-[4-(4-acetamidophenyl)sulfanylphenoxy]phenyl]sulfanylphenyl]acetamide is a complex organic compound with the molecular formula C28H24N2O4S2. It is a derivative of acetamide, featuring a long chain of phenyl rings and sulfanyl groups. The compound is characterized by the presence of an acetamide group at one end and a series of phenyl rings connected through sulfanyl bridges. The central phenyl ring has a 4-acetamidophenyl group attached, which contributes to its chemical properties. N-[4-[4-[4-(4-acetamidophenyl)sulfanylphenoxy]phenyl]sulfanylphenyl]acetamide is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential for specific interactions with biological targets.

5186-55-0

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5186-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5186-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5186-55:
(6*5)+(5*1)+(4*8)+(3*6)+(2*5)+(1*5)=100
100 % 10 = 0
So 5186-55-0 is a valid CAS Registry Number.

5186-55-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-[4-[4-(4-acetamidophenyl)sulfanylphenoxy]phenyl]sulfanylphenyl]acetamide

1.2 Other means of identification

Product number -
Other names -

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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More Details:5186-55-0 SDS

5186-55-0Relevant academic research and scientific papers

Synthesis, tautomeric structure, dyeing characteristics, and antimicrobial activity of Novel 4-(2-arylazophenyl)-3-(2-hydroxyphenyl)-1-phenyl-2-pyrazolin- 5-ones

Metwally,Bondock,El-Desouky,Abdou

experimental part, p. 82 - 91 (2012/05/04)

Novel azopyrazolin-5-one dyes 4a-f were synthesized by the regioselective reaction of phenylhydrazine with 2,3,4-chromantrione-3-arylhydrazones 2a-f. The acid dissociation constants pKa for the series prepared were determined and correlated by the Hammett equation. The results of such correlation together with the spectral data indicated that the studied compounds exist predominantly in the hydrazone keto structure, (D) as the Z-configuration. The dyes were applied to polyester fabrics, affording orange-yellow shades and assessments of their dyeing performance are considered. Further, the compounds 4a-f were screened for their antimicrobial activity against various microorganisms.

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