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1-Methyl-2,5-bis-phenylsulfanylmethyl-1H-pyrrole is a monomer derived from the bis(phenylthiomethylene) functionalization of 1-methylpyrrole, synthesized via a Mannich reaction followed by substitution with sodium thiophenoxide. It serves as a precursor for low band gap conductive polymers through base-induced elimination of thiophenyl groups, enabling the formation of conjugated polymer structures.

203071-36-7

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203071-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 203071-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,0,7 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 203071-36:
(8*2)+(7*0)+(6*3)+(5*0)+(4*7)+(3*1)+(2*3)+(1*6)=77
77 % 10 = 7
So 203071-36-7 is a valid CAS Registry Number.

203071-36-7Downstream Products

203071-36-7Relevant academic research and scientific papers

Solution processible poly(l-alkyl-2,5-pyrrolenevinylenes): New low band gap conductive polymers

Kim, In Tae,Elsenbaumer, Ronald L.

, p. 327 - 328 (1998)

Bis(phenylthiomethylene) derivatives of 1-alkylpyrroles afford conjugated polymers by base induced elimination of thiophenyl groups.

Convenient synthesis of 1-alkyl-2,5-bis(thiophenylmethylene)pyrroles using the mannich reaction

Kim, In Tae,Elsenbaumer, Ronald L.

, p. 1087 - 1090 (1998)

Aminomethylation of 1-alkylpyrrole (alkyl: hydrogen, methyl, hexyl, dodecyl) by aqueous formaldehyde and dimethylamine hydrochloride, followed by reaction with iodomethane, affords the 1-alkyl-2,5-bis[(trimethylamino) methyl]pyrrole diiodide. These diiodide salt derivatives react with sodium thiophenoxide to give 1-alkyl-2,5-bis(thiophenyl methylene) pyrrole yielding monomers found to be useful for synthesizing new conducting polymers.

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