1144503-29-6

Basic information

• Product Name: dimethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2,5-dicarboxylate
• Synonyms: dimethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2,5-dicarboxylate
• CAS NO: 1144503-29-6
• Molecular Weight: 455.464
• Mol File: 1144503-29-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: dimethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2,5-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2,5-dicarboxylate(1144503-29-6)
• EPA Substance Registry System: dimethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2,5-dicarboxylate(1144503-29-6)

Safety Data

• Hazardous Substances Data: 1144503-29-6(Hazardous Substances Data)

Upstream product

• 1265221-54-2 dimethyl 3,4-diiodo-1H-pyrrole-2,5-dicarboxylate 
• 122775-35-3 3,4-Dimethoxyphenylboronic acid 
• 473401-82-0 pyrrole-1,2,5-tricarboxylic acid 1-tert-butyl ester 2,5-dimethyl ester 
• 1431884-48-8 methyl (E)-2-hydrazono-3-(3,4-dimethoxyphenyl)propionate 
• 1431884-61-5 C₁₂H₁₄N₂O₄ 
• 1144503-23-0 dimethyl N-benzyl-3,4-bis(3,4-dimethoxyphenyl)pyrrole-2,5-dicarboxylate 

Relevant articles and documents

Design and synthesis of 3,4-diarylpyrrole analogues as potent topoisomerase inhibitors

Background: The natural products containing a common 3,4-diarylpyrrole skeleton have attracted considerable attention due to their unique structures and multiplex biological activities. In our previous study, lycogarubin C was synthesized and showed cytot

A general method for the synthesis of N-unsubstituted 3,4-diarylpyrrole-2, 5-dicarboxylates

A general method for the synthesis of N-unsubstituted 3,4-diarylpyrrole-2, 5-dicarboxylates (3) has been developed. The key reactions involved are the Hinsberg-type synthesis of dimethyl N-benzyl-3,4-dihydroxypyrrole-2,5- dicarboxylate (6) followed by palladium-catalyzed Suzuki-Miyaura coupling of its bis-triflate derivative (7). The N-benzyl protecting group of the resulting 3,4-diaryl pyrrole-2,5-dicarboxyl ates (8) is cleanly removed under hydrogenolytic or solvolytic conditions.