53979-33-2

Upstream product

• 7350-60-9 3-(3,4-dimethoxyphenyl)-2-methylacrylic acid 
• 107150-69-6 (E)-3-(3,4-dimethoxyphenyl)-2-methylacrylic acid methyl ester 
• 64-18-6 formic acid 
• 93-15-2 1,2-dimethoxy-4-(2-propenyl)benzene 
• 1373333-25-5 (S)-4-benzyl-3-(3-(3,4-dimethoxyphenyl)propanoyl)-oxazolidin-2-one 
• 1373333-26-6 (R)-4-benzyl-3-(3-(3,4-dimethoxyphenyl)propanoyl)-oxazolidin-2-one 
• 51842-87-6 3-(3,4-dimethoxy-phenyl)-propionyl chloride 
• 2107-70-2 3,4-methoxycinnamic acid 
• 1373333-40-4 (R)-4-benzyl-3-(3-(3,4-dimethoxyphenyl)propanoyl)-oxazolidin-2-one 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 4191-17-7 5,6-dimethoxy-2- methyl-2,3-dihydro-1H-inden-1-one 
• 106273-88-5 3-(3,4-dimethoxy-phenyl)-2-methyl-propionic acid amide 
• 148149-47-7 3-(3,4-dimethoxy-phenyl)-2-methyl-propionic acid methyl ester 
• 859188-87-7 3-(2-bromo-4,5-dimethoxy-phenyl)-2-methyl-propionic acid 
• 7306-32-3 (S)-3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid 
• 7306-32-3 (R)-3-(3,4-dimethoxyphenyl)-2-methylpropanoic acid 
• 77531-73-8 3-(3,4-dimethoxyphenyl)-2-methylpropan-1-ol 
• 21727-03-7 4-(3-bromo-2-methylpropyl)-1,2-dimethoxybenzene 
• 1315172-38-3 1,2-dimethoxy-4-(2-methyl-3-nitropropyl)benzene 
• 1315172-40-7 2-(4,5-dimethoxy-2-(2-methyl-3-nitropropyl)benzoyl)benzoic acid 
• 1315172-42-9 C₂₁H₂₃NO₇ 
• 7306-29-8 (S)-4-(3,4-dimethoxyphenyl)-3-methyl-2-butanone 
• 1386447-03-5 C₁₃H₁₉NO₃ 
• 100388-95-2 (S)-3-(3,4-dimethoxy-phenyl)-2-methyl-propionyl chloride 

Relevant academic research and scientific papers

Pd-Catalyzed Regioselective Branched Hydrocarboxylation of Terminal Olefins with Formic Acid

A regioselective Pd-catalyzed hydrocarboxylation of terminal olefins with HCOOH is described. A wide variety of branched carboxylic acids can readily be obtained with high regioselectivities under mild reaction conditions. The reaction is operationally simple and requires no handling of toxic CO. The ligand and LiCl are important factors for reaction reactivity and selectivity.

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.

Concise synthesis of 2-benzazepine derivatives and their biological activity

Figure Persented: 2-Benzazepines, which are potentially good candidates for new drug therapies to treat skin wounds, were readily prepared from substituted cinnamylamide via an intramolecular Friedel-Crafts reaction. With few steps and effective reactions

Probing the steric space at the floor of the D1 dopamine receptor orthosteric binding domain: 7α-, 7β-, 8α-, and 8β-methyl substituted dihydrexidine analogues

To probe the space at the floor of the orthosteric ligand binding site in the dopamine D1 receptor, four methylated analogues of dihydrexidine (DHX) were synthesized with substitutions at the 7 and 8 positions. The 8α-axial, 8β-equatorial, and