1159581-63-1

Basic information

• Product Name: tert-butyl 4-iodo-2-(4-methoxy-phenyl)-1H-pyrrole-1-carboxylate
• Synonyms: tert-butyl 4-iodo-2-(4-methoxy-phenyl)-1H-pyrrole-1-carboxylate
• CAS NO: 1159581-63-1
• Molecular Weight: 399.228
• Mol File: 1159581-63-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: tert-butyl 4-iodo-2-(4-methoxy-phenyl)-1H-pyrrole-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 4-iodo-2-(4-methoxy-phenyl)-1H-pyrrole-1-carboxylate(1159581-63-1)
• EPA Substance Registry System: tert-butyl 4-iodo-2-(4-methoxy-phenyl)-1H-pyrrole-1-carboxylate(1159581-63-1)

Safety Data

• Hazardous Substances Data: 1159581-63-1(Hazardous Substances Data)

Upstream product

• 198981-85-0 2-(4-methoxyphenyl)-1H-pyrrole-1-carboxylic acid 1,1-dimethylethyl ester 
• 100-07-2 4-methoxy-benzoyl chloride 
• 92136-39-5 N-tert-Butoxycarbonyl-1-amino-3-propyne 
• 1159581-59-5 tert-butyl 4-(4-methoxyphenyl)-4-oxobut-2-yn-1-ylcarbamate 

Downstream Products

• 1159581-72-2 tert-butyl 4-(2-(triisopropylsilyl)ethynyl)-2-(4-methoxyphenyl)-1H-pyrrole-1-carboxylate 
• 1159581-73-3 tert-butyl 2-(4-methoxyphenyl)-4-(2-phenylethynyl)-1H-pyrrole-1-carboxylate 
• 1266358-08-0 tert-butyl 4-(4-{1-[(tert-butoxy)carbonyl]-5-(4-methoxyphenyl)-1H-pyrrol-3-yl}buta-1,3-diyn-1-yl)-2-(4-methoxyphenyl)-1H-pyrrole-1-carboxylate 
• 1316228-27-9 C₂₂H₂₂N₄O₂ 
• 1333469-94-5 2,5-bis(5-(4-methoxyphenyl)-1H-pyrrol-3-yl)pyrimidine 

Relevant articles and documents

One-pot synthesis of diazine-bridged bisindoles and concise synthesis of the marine alkaloid hyrtinadine A

Diazine-bridged bisindoles are readily obtained from N-Bocprotected 3-iodoindoles and 3-iodo-7-azaindole in a pseudo three-component reaction involving a one-pot Masuda borylation-Suzuki arylation sequence. Some of the title com-pounds display promising c

Rapid synthesis of bis(hetero)aryls by one-pot Masuda borylation-Suzuki coupling sequence and its application to concise total syntheses of meridianins A and G

3-(Hetero)aryl substituted indoles, 7-azaindoles, and pyrroles can be obtained in a very concise fashion via a one-pot Masuda borylation-Suzuki coupling sequence. The concise total syntheses of the marine natural products meridianins A (5) and G (4i) nice

Three-component synthesis of N-boc-4-iodopyrroles and sequential one-pot alkynylation

(Hetero)aryl-, alkenyl-, and selected alkyl-substituted acid chlorides can be efficiently coupled with N-Boc-protected propargylamine to produce ynones which are converted in a one-pot fashion to 2-substituted N-Boc-4-iodopyrroles. Upon addition of a furt