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Diethyl 5-{[(4-chloro-2-methylphenoxy)acetyl]amino}-3-methylthiophene-2,4-dicarboxylate is a complex organic compound with the molecular formula C22H22ClNO5S. It is characterized by a thiophene ring, which is a five-membered aromatic ring with one sulfur atom, and a dicarboxylate group, indicating the presence of two carboxylate groups. The compound also features a 4-chloro-2-methylphenoxy acetyl moiety, which is an amide derivative of a chlorinated and methylated phenol. This structure contributes to the compound's potential pharmaceutical or chemical applications, as it may exhibit specific biological activities or reactivity. The diethyl ester group suggests that the compound is likely soluble in organic solvents and may be used in the synthesis of other compounds or as an intermediate in chemical reactions. Overall, diethyl 5-{[(4-chloro-2-methylphenoxy)acetyl]amino}-3-methylthiophene-2,4-dicarboxylate's structure indicates a potential for use in various chemical or pharmaceutical contexts, though its specific applications would depend on further research and testing.

6147-96-2

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6147-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6147-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6147-96:
(6*6)+(5*1)+(4*4)+(3*7)+(2*9)+(1*6)=102
102 % 10 = 2
So 6147-96-2 is a valid CAS Registry Number.

6147-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 5-[[2-(4-chloro-2-methylphenoxy)acetyl]amino]-3-methylthiophene-2,4-dicarboxylate

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:6147-96-2 SDS

6147-96-2Downstream Products

6147-96-2Relevant academic research and scientific papers

Naphthofuranone Derivatives as Specific Inhibitors of Thymidylate Synthases

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Page/Page column 5, (2010/03/31)

Synthetic compounds of 1,2-naphthalein moelcules (I) having specific inhibitory properties of the enzymatic activity of thymidylate synthases of bacterial species, their preparation, their pharmaceutical composition and use in the treatment and prophylaxi

NAPHTHOFURANONE DERIVATIVES AS SPECIFIC INHIBITORS OF THYMIDYLATE SYNTHASES

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Page/Page column 10-11, (2008/06/13)

Synthetic compounds of 1, 2 -naphthalein molecules (I) having specific inhibitory properties of the enzymatic activity of thymidylate synthases of bacterial species, their preparation, their pharmaceutical composition and use in the treatment and prophyla

Antibacterial agent discovery using thymidylate synthase biolibrary screening

Costi, M. Paola,Gelain, Arianna,Barlocco, Daniela,Ghelli, Stefano,Soragni, Fabrizia,Reniero, Fabiano,Rossi, Tiziana,Ruberto, Antonio,Guillou, Claude,Cavazzuti, Antonio,Casolari, Chiara,Ferrari, Stefania

, p. 5958 - 5968 (2007/10/03)

Thymidylate synthase (TS, Thy A) catalyzes the reductive methylation of 2′-deoxyuridine 5′-monophosphate to 2′-deoxythymidine 5′-monophosphate, an essential precursor for DNA synthesis. A specific inhibition of this enzyme induces bacterial cell death. As

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