29113-73-3

Basic information

• Product Name: 3-Furancarboxylic acid, 2-methyl-5-phenyl-, methyl ester
• CAS NO: 29113-73-3
• Molecular Formula: C13H12O3
• Molecular Weight: 216.236
• Mol File: 29113-73-3.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 3-Furancarboxylic acid, 2-methyl-5-phenyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Furancarboxylic acid, 2-methyl-5-phenyl-, methyl ester(29113-73-3)
• EPA Substance Registry System: 3-Furancarboxylic acid, 2-methyl-5-phenyl-, methyl ester(29113-73-3)

Safety Data

• Hazardous Substances Data: 29113-73-3(Hazardous Substances Data)

Upstream product

• 75519-85-6 5-methoxycarbonyl-4-methyl-1-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene 
• 4747-15-3 1-(2-methoxyvinyl)benzene 
• 105-45-3 acetoacetic acid methyl ester 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 33440-88-9 silver phenylacetylide 
• 536-74-3 phenylacetylene 
• 96-09-3 styrene oxide 
• 122-78-1 phenylacetaldehyde 
• 108-86-1 bromobenzene 
• 6141-58-8 methyl 2-methyl-3-furancarboxylate 
• 24762-04-7 2-Diazo-3-oxo-butyric acid methyl ester 
• 345891-28-3 methyl 5‐bromo‐2‐methylfuran‐3‐carboxylate 
• 98-80-6 phenylboronic acid 

Downstream Products

• 41167-64-0 methyl 2-acetyloxy-4-oxo-4-phenylbutenoate 
• 78752-46-2 methyl (E)-2-acetyl-3-benzoyl-2,3-epoxypropionate 
• 1334598-00-3 C₁₉H₁₈N₂O₂S 
• 108124-17-0 2-methyl-5-phenyl-furan-3-carboxylic acid 
• 1176256-25-9 methyl [3-({[4-(4-methoxyphenyl)-2-methyl-5-phenylfuran-3-yl]carbonyl}amino)phenoxy]acetate 
• 1176256-76-0 4-(4-methoxyphenyl)-2-methyl-5-phenylfuran-3-carboxylic acid 
• 1176256-75-9 methyl 4-(4-methoxyphenyl)-2-methyl-5-phenylfuran-3-carboxylate 
• 1176256-74-8 methyl 4-bromo-2-methyl-5-phenylfuran-3-carboxylate 
• 90043-44-0 (3R,3aR,6aS)-5-Methyl-2-oxo-6a-phenyl-2,3,3a,6a-tetrahydro-furo[2,3-b]furan-3,4-dicarboxylic acid dimethyl ester 
• 90043-53-1 methyl 2-acetyl-3-benzoylpropenoate 
• 75519-89-0 2-hydroperoxy-5-methoxy-3-methoxycarbonyl-2-methyl-5-phenyldihydrofuran 
• 75519-87-8 methyl (E)-2-acetyl-3-benzoylacrylate 
• 75519-85-6 5-methoxycarbonyl-4-methyl-1-phenyl-2,3,7-trioxabicyclo<2.2.1>hept-5-ene 

Relevant articles and documents

Direct (Hetero)arylation of Heteroarenes Catalyzed by Unsymmetrical Pd-PEPPSI-NHC Complexes under Mild Conditions

With the aim of developing a facile and efficient method to access structurally intriguing and valuable functionalized (hetero)aryls, two unsymmetrical Pd-PEPPSI-type NHC complexes (PEPPSI, pyridine-enhanced precatalyst preparation, stabilization, and initiation; NHC, N-heterocyclic carbene) were designed and synthesized to catalyze the direct arylation of heteroarenes with (hetero)aryl bromides. The results demonstrated that the utilization of this "unsymmetrical"strategy led to much higher efficiency in comparison to the commonly used C2-symmetric Pd-PEPPSI-type NHC complexes. Furthermore, a broad range of heteroaromatics and (hetero)aryl bromide partners with a wide variety of functional groups were all amenable to the developed protocol even at as low as 0.05 mol % catalyst loading and under aerobic conditions. More importantly, along with our study, we also found that the present protocol could provide expedient access to the gram-scale synthesis of the muscle relaxant drug dantrolene and conjugated mesopolymers.

Palladium Complexes with Tetrahydropyrimidin-2-ylidene Ligands: Catalytic Activity for the Direct Arylation of Furan, Thiophene, and Thiazole Derivatives

The synthesis and characterization of novel 1,3-benzyl-3,4,5,6-tetrahydropyrimidin-2-ylidene-based N-heterocyclic carbene palladium(II) complexes (1a-d) were described. The crystal structure of trans-dichlorobis[1,3-bis(4-methylbenzyl)-3,4,5,6-tetrahydrop

Cobalt(II)-catalyzed electrophilic alkynylation of 1,3-dicarbonyl compounds to form polysubstituted furans via π-π Activation

Polysubstituted furans were obtained with excellent yields via the electrophilic alkynylation of 1,3-dicarbonyl compoundsws with phenyl- or ester-substituted brominated alkynes. The reaction is catalyzed by the inexpensive and readily available catalyst, cobalt(II) chloride, and has a wide substrate scope. The C(sp)-C(sp3) coupling occurs under mild conditions with short reaction times and does not require an inert atmosphere or ligands. It is proposed that the reaction proceeds through a chelation complex of cobalt(II) with the deprotonated 1,3-dicarbonyl compound.