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N-(2-methoxyphenyl)-2-{3-[(phenylcarbonyl)carbonohydrazonoyl]phenoxy}acetamide is a complex organic compound with the molecular formula C22H20N2O5. It is a derivative of acetamide, featuring a 2-methoxyphenyl group attached to the nitrogen atom, and a phenoxy group connected to the acetamide backbone through a carbonyl linker. The phenoxy group is further substituted with a 3-[(phenylcarbonyl)carbonohydrazonoyl] moiety, which adds to the molecule's complexity. N-(2-methoxyphenyl)-2-{3-[(phenylcarbonyl)carbonohydrazonoyl]phenoxy}acetamide is characterized by its potential applications in pharmaceutical research, particularly in the development of new drugs, due to its unique structure and the presence of multiple functional groups that can interact with biological targets.

5439-74-7

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5439-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5439-74-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5439-74:
(6*5)+(5*4)+(4*3)+(3*9)+(2*7)+(1*4)=107
107 % 10 = 7
So 5439-74-7 is a valid CAS Registry Number.

5439-74-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(5-methyl-2-propan-2-ylphenoxy)-sulfanyl-sulfanylidene-$l^{5}-phosphane

1.2 Other means of identification

Product number -
Other names tetra-N-ethyl-3,6,9-trioxa-undecanediyldiamine

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:5439-74-7 SDS

5439-74-7Relevant academic research and scientific papers

Dithiophosphoric and dithiophosphonic acids and their derivatives on the basis of thymol: Synthesis and antimicrobial activity

Cherkasov, Rafael A.,Nizamov, Ilyas S.,Gabdullina, Gulnara T.,Almetkina, Lyubov A.,Shamilov, Radik R.,Sofronov, Artem V.

, p. 33 - 35 (2013/07/19)

Biologically active dithiophosphoric and dithiophosphonic acids, their ammonium salts as well as S-silyl and S-plumbyl derivatives were prepared by the reaction of thymol with tetraphosphorus decasulfide and 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disu

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