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3'-methoxy-2,2':5',2-terthiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58930-53-3

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58930-53-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58930-53-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,3 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58930-53:
(7*5)+(6*8)+(5*9)+(4*3)+(3*0)+(2*5)+(1*3)=153
153 % 10 = 3
So 58930-53-3 is a valid CAS Registry Number.

58930-53-3Downstream Products

58930-53-3Relevant academic research and scientific papers

CONVENIENT SYNTHESIS OF VARIOUS TERHETEROCYCLIC COMPOUNDS BY Pd(O)-CATALYZED COUPLING REACTIONS

Gronowitz, Salo,Peters, Dan

, p. 645 - 658 (1990)

Various terheterocyclic compounds containing thiophene, furan, selenophene, pyridine and thiazole rings have been obtained by the Pd(PPh3)4-catalyzed coupling of dihalo-substituted heterocyclic compounds with heterocyclic boronic acids, using sodium bicar

SYNTHESIS AND CHARACTERIZATION OF 2,2':5',2''-TERTHIOPHENE DERIVATIVES OF POSSIBLE THERAPEUTIC USE

Rossi, Renzo,Carpita, Adriano,Ciofalo, Maurizio,Houben, Julien L.

, p. 793 - 803 (2007/10/02)

Several derivatives of 2,2':5',2''-terthiophene, 1a, and a structural analogue of this natural phototoxin, i.e. 5--2,2'-bithiophene, 2, have been conveniently synthesized on a medium scale using a general approach which involves palladium-catalyzed carbon-carbon bond forming reactions between (hetero)aryl halides and heteroaryl organometallics such as Grignard reagents, organozinc and organotin compounds.These 2,2':5',2''-terthiophene derivatives, which include some naturally-occurring compounds, have been characterized by EIMS spectrometry , 1H and 13C NMR spectroscopy as well as by absorption and fluorescence measurements.Four of these phototoxins exhibit considerable antibiotic and antiviral properties in the presence of UVA light and are cytotoxic against the P 815 mouse mastocytoma cell line.

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