97302-05-1

Basic information

• Product Name: Zinc, bis(4-methoxyphenyl)-
• CAS NO: 97302-05-1
• Molecular Formula: C14H14O2Zn
• Molecular Weight: 279.654
• Mol File: 97302-05-1.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Zinc, bis(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Zinc, bis(4-methoxyphenyl)-(97302-05-1)
• EPA Substance Registry System: Zinc, bis(4-methoxyphenyl)-(97302-05-1)

Safety Data

• Hazardous Substances Data: 97302-05-1(Hazardous Substances Data)

Upstream product

• 1263387-17-2 C₁₀H₁₆N₂O₃S 
• 93296-09-4 4-methoxyphenylzinc chloride 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 7699-45-8 zinc dibromide 
• 7646-85-7 zinc(II) chloride 
• 696-62-8 para-iodoanisole 

Downstream Products

• 1283129-20-3 2,3,4,6-tetra-O-pivaloyl 1-(2-anisyl)-1-deoxy-β-D-glucopyranose 
• 1574486-21-7 3-hydroxy-3-(4-methoxyphenyl)-2-(pyridin-2-yl)isoindolin-1-one 
• 1574486-26-2 5-hydroxy-5-(4-methoxyphenyl)-3,4-dimethyl-1-(pyridin-2-yl)-1H-pyrrol-2(5H)-one 
• 658-17-3 1-(methoxy)-4-(difluoromethyl)benzene 
• 613-37-6 4-methoxylbiphenyl 
• 1283526-92-0 4-(4-methoxyphenyl)-4-methyltetrahydro-2H-pyran 
• 2948-44-9 1-methoxy-4-(1-methylcyclohexyl)benzene 
• 1562-28-3 1-methoxy-4-(1-methylcyclopentyl)benzene 

Relevant articles and documents

Direct C-C bond construction from arylzinc reagents and aryl halides without external catalysts

Direct cross-coupling between an arylzinc reagent and an aryl halide was accomplished without any external catalyst, enabling efficient and selective formation of the corresponding biaryl compound with broad functional group compatibility. Direct cross-coupling between a diarylzinc compound and an aryl iodide was accomplished without using any external catalyst. The reaction is efficient and selective, enabling formation of the corresponding biaryl compounds with broad functional group compatibility. The reaction is proposed to proceed by a thermally initiated single electron transfer (SET) route. Copyright

FARNESOID X RECEPTOR AGONISTS AND USES THEREOF

Described herein are compounds that are farnesoid X receptor agonists, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with farnesoid X receptor activity.

Quaternary Centers by Nickel-Catalyzed Cross-Coupling of Tertiary Carboxylic Acids and (Hetero)Aryl Zinc Reagents

This work bridges a gap in the cross-coupling of aliphatic redox-active esters with aryl zinc reagents. Previously limited to primary, secondary, and specialized tertiary centers, a new protocol has been devised to enable the coupling of general tertiary systems using nickel catalysis. The scope of this operationally simple method is broad, and it can be used to simplify the synthesis of medicinally relevant motifs bearing quaternary centers.