13048-81-2

Basic information

• Product Name: (Z)-3-(4-methoxyphenyl)-2-methylacrylic acid
• Synonyms: (Z)-3-(4-methoxyphenyl)-2-methylacrylic acid
• CAS NO: 13048-81-2
• Molecular Weight: 192.214
• Mol File: 13048-81-2.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: (Z)-3-(4-methoxyphenyl)-2-methylacrylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3-(4-methoxyphenyl)-2-methylacrylic acid(13048-81-2)
• EPA Substance Registry System: (Z)-3-(4-methoxyphenyl)-2-methylacrylic acid(13048-81-2)

Safety Data

• Hazardous Substances Data: 13048-81-2(Hazardous Substances Data)

Upstream product

• 1039703-99-5 ethyl (2E)-3-(4-methoxyphenyl)-2-[(trimethylsilyl)methyl]prop-2-enoate 
• 516-05-2 methyl-propanedioic acid 
• 591-31-1 3-methoxy-benzaldehyde 
• 1039703-89-3 ethyl (2Z)-3-(4-methoxyphenyl)-2-[(trimethylsilyl)methyl]prop-2-enoate 
• 1367876-22-9 [(Z)-2-methoxycarbonyl-3-(4-methoxyphenyl)-2-propenyl]triphenylphosphonium bromide 
• 64-18-6 formic acid 
• 2749-94-2 1-methoxy-4-(prop-1-yn-1-yl)benzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 52750-05-7 ethyl (E)-3-(4-methoxyphenyl)-2-methylpropenoate 
• 213999-88-3 methyl (2Z)-2-(bromomethyl)-3-(4-methoxyphenyl)prop-2-enoate 
• 137-40-6 sodium proprionate 
• 144-55-8 sodium hydrogencarbonate 
• 115240-92-1 methyl 2-[hydroxy(4-methoxyphenyl)methyl]prop-2-enoate 
• 126356-04-5 (E)-methyl 2-methyl-3-(p-methoxyphenyl)prop-2-enoate 

Downstream Products

• 52427-11-9 3-(4-methoxyphenyl)-2-methylpropionic acid 
• 61227-51-8 3-(3-methoxyphenyl)-2-methylpropionic acid 
• 353476-46-7 (E)-N-methoxy-N-methyl-3-(4-methoxyphenyl)-2-methyl-acrylamide 
• 122-84-9 4-methoxybenzyl methyl ketone 
• 1228457-91-7 ethyl (1S,5S)-1-ethyl-3-hydroxy-5-(4-methoxyphenyl)-4-methyl-2-oxocyclopent-3-enecarboxylate 
• 1228457-77-9 ethyl (E)-2-ethyl-6-(4-methoxyphenyl)-5-methyl-3,4-dioxohex-5-enoate 

Relevant articles and documents

Copper-Photocatalyzed Contra-Thermodynamic Isomerization of Polarized Alkenes

The contra-thermodynamic isomerization of α- and β-substituted cinnamate derivatives catalyzed by the Cu(OAc)2/rac-BINAP complex under blue light irradiation is reported. The use of an oxazolidinone template, which favored the complexation of the copper catalyst to the substrate, allowed the E → Z isomerization of the catalytically formed chromophore under simple and robust reaction conditions in good to excellent ratios. The mechanism of this process based on the transient formation of a chromophore was also studied.

DERIVATIVES OF SULINDAC CAN PROTECT NORMAL CELLS AGAINST OXIDATIVE DAMAGE

The disclosure provides chemical compounds possessing therapeutic and/or protective properties against oxidative damage. Methods of making such therapeutic and/or protective compounds and associated compositions are also provided, as are methods for their use, which include protecting cells from oxidative damage and/or inhibiting production of ROS in a cell or subject, as well as preventing or reducing the extent of tissue damage caused by an ischemic event in a subject at elevated risk of such an event.