17595-85-6

Basic information

• Product Name: methyl 3-(thiophen-2-yl)benzoate
• Synonyms: methyl 3-(thiophen-2-yl)benzoate
• CAS NO: 17595-85-6
• Molecular Weight: 218.276
• Mol File: 17595-85-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 3-(thiophen-2-yl)benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(thiophen-2-yl)benzoate(17595-85-6)
• EPA Substance Registry System: methyl 3-(thiophen-2-yl)benzoate(17595-85-6)

Safety Data

• Hazardous Substances Data: 17595-85-6(Hazardous Substances Data)

Upstream product

• 1003-09-4 2-bromothiophene 
• 99769-19-4 [3-(methoxycarbonyl)phenyl]boronic acid 
• 618-89-3 methyl 3-bromobenzoate 
• 15106-95-3 bis(thien-2-yl)zinc 
• 67-56-1 methanol 

Downstream Products

• 29886-63-3 3-(thiophen-2-yl)benzoic acid 

Relevant articles and documents

A sustainable heterogenized palladium catalyst for Suzuki-Miyaura cross coupling reaction of azaheteroaryl halides in aqueous media

A unique recyclable Pd catalyst (‘SiO2’-NH2-Pd) for Suzuki-Miyaura coupling reaction of azaheteroaryl halides is developed. The catalytic system is working under mild aqueous condition with low Pd loading and without the use of phosphine ligand. The plausible mechanism is proposed based on the formation of undesired symmetrical biaryl from the coupling reaction of azaheteroaryl chlorides due to the oxidative homocoupling of nucleophilic arylboronic acid. This catalytic system represents an attractive and promising approach for the synthesis of azaheterobiaryls with high product yields. The catalyst has demonstrated an excellent recyclability.

Erratum: Negishi cross-coupling reaction catalyzed by an aliphatic, phosphine based pincer complex of palladium. biaryl formation via cationic pincer-type PdIV intermediates (Dalton Transactions (2011) 40 (8996) DOI: 10.1039/C1DT10398A)

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