115510-90-2

Basic information

• Product Name: N-(2'-amino-[1,1'-binaphthalen]-2-yl)acetamide
• CAS NO: 115510-90-2
• Molecular Weight: 326.398
• Mol File: 115510-90-2.mol

Chemical Properties

• CAS DataBase Reference: N-(2'-amino-[1,1'-binaphthalen]-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2'-amino-[1,1'-binaphthalen]-2-yl)acetamide(115510-90-2)
• EPA Substance Registry System: N-(2'-amino-[1,1'-binaphthalen]-2-yl)acetamide(115510-90-2)

Safety Data

• Hazardous Substances Data: 115510-90-2(Hazardous Substances Data)

Upstream product

• 4488-22-6 1,1'-binaphthalene-2,2'-diamine 
• 108-24-7 acetic anhydride 
• 20191-75-7 1-bromo-2-naphthylamine 
• 4488-22-6 (+)-(R)-1,1'-binaphthyl-2,2'-diamine 
• 75-36-5 acetyl chloride 

Downstream Products

• 86688-06-4 (R_a)-2,2'-diiodo-1,1'-binaphthyl 

Relevant articles and documents

Hexafluoroisopropanol-Enabled Copper-Catalyzed Asymmetric Halogenation of Cyclic Diaryliodoniums for the Synthesis of Axially Chiral 2,2′-Dihalobiaryls

An efficient asymmetric halogenation of cyclic diaryliodonium salts is demonstrated, which gives access to a wide range of axially chiral 2,2′-dihalobiaryls in good to excellent yields and with excellent enantioselectivities. The use of CuX with chiral bisoxazoline ligand and tetrabutylammonium halides in the unique solvent of hexafluoroisopropanol (HFIP) led to the best results in the process. The axially chiral 2,2′-dihalobiaryls can be transformed into a number of enantiopure chiral ligands that could be potentially useful in asymmetric catalysis.

Modular metal-carbon stabilized palladium nanoparticles for the catalytic hydrogenation of N-heterocycles

We report here the first modular metal-carbon stabilized palladium nanoparticles based on binaphthyl scaffolds, which can be prepared from palladium salts and substituted binaphthyl diazonium salts in homogeneous system through direct reduction using sodium borohydride. The resulting palladium nanoparticles subjected to the electron density of modular moieties are found to be novel and efficient catalysts for the catalytic hydrogenation of N-heterocycles, affording the corresponding adducts in good to excellent yields under mild conditions.

Enantioselective Cyclopropanation of 1,1-Diphenylethylene and Diazoacetic Acid Ester with Copper Catalysts

Copper(II) compounds catalyze the reaction of 1,1-diphenylethylene with diazoacetic acid ethylester.The main product is 2,2-diphenylcyclopropane carboxylic acid ethylester.The formation of the carbene dimerization products fumaric and maleic acid diethylester can be suppressed by the continuous addition of diazoacetic ester to 1,1-diphenylethylene. 37 optically active ligands, partly new, were combined with copper(II)-acetate to give in-situ-catalysts.In five cases isolated copper complexes were used as catalysts.The best optical inductions in the formation of 2,2-diphenylcyclopropane carboxylic acid ethylester with up to 65.6percent ee were achived with Schiffbase ligands, which derive from salicylaldehyde and amino alcohols, obtained from amino acid esters and phenyl Grignard. - Keywords: Catalytic enantioselective cyclopropanation; Copper(II) catalysts; Optical induction.