29325-49-3

Basic information

• Product Name: N,N'-(1,1'-Biphenyl-2,2'-diyl)bisacetamide
• Synonyms: N,N'-(1,1'-Biphenyl-2,2'-diyl)bisacetamide
• CAS NO: 29325-49-3
• Molecular Formula: C₁₆H₁₆N₂O₂
• Molecular Weight: 0
• Mol File: 29325-49-3.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N,N'-(1,1'-Biphenyl-2,2'-diyl)bisacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(1,1'-Biphenyl-2,2'-diyl)bisacetamide(29325-49-3)
• EPA Substance Registry System: N,N'-(1,1'-Biphenyl-2,2'-diyl)bisacetamide(29325-49-3)

Safety Data

• Hazardous Substances Data: 29325-49-3(Hazardous Substances Data)

Upstream product

• 1454-80-4 1,1'-biphenyl-2,2'-diamine 
• 108-24-7 acetic anhydride 
• 19591-17-4 o-iodoacetanilide 
• 2436-96-6 1-nitro-2-(2-nitrophenyl)benzene 
• 34801-09-7 N-(2-aminophenyl)acetamide 
• 614-76-6 N-acetyl-2-bromoaniline 
• 615-36-1 2-bromoaniline 
• 14040-11-0 tungsten hexacarbonyl 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 873792-52-0 5,5′-dibromo-2,2′-diiodo-1,1′-biphenyl 
• 86-71-5 3,6-diamino-9H-carbazole 
• 61837-20-5 5,5'-dinitro-biphenyl-2,2'-diyldiamine 
• 1127231-62-2 2',2''-diacetylamino-m-quaterphenyl 
• 1454-80-4 1,1'-biphenyl-2,2'-diamine 
• 86-74-8 9H-carbazole 

Relevant articles and documents

A novel construction of acetamides from rhodium-catalyzed aminocarbonylation of DMC with nitro compounds

Dimethyl carbonate (DMC), an environment-friendly compound prepared from CO2, shows diverse reactivities. In this communication, an efficient procedure using DMC as both a C1 building block and solvent in the aminocarbonylation reaction with nitro compounds has been developed. W(CO)6acts both a CO source and a reductant here.

A modified Cu(0)-Cu(I)-mediated Caryl-CarylUllmann coupling for the synthesis of biaryls

A novel Cu(0)-Cu(I)-mediated Caryl-CarylUllmann coupling has been successfully developed. The use of Cu(I) salts allowed the reactions to proceed under relatively mild conditions (65?°C in DMSO for 15–72?h). The developed method was compatible with a relatively wide range of functional groups simultaneously present on the aromatic ring of different electronic nature. The aryl halides with an electron-withdrawing group ortho to the halide or an electron-donating group meta or para to the halide furnished the corresponding products in good to excellent yields (up to 98%).

Design and synthesis of novel ROR inverse agonists with a dibenzosilole scaffold as a hydrophobic core structure

Abstract Molecular structure calculations indicated that the dibenzosilole skeleton could be well superposed on phenanthridinone, which is a structural component of ligands of retinoic acid receptor-related orphan receptors (RORs). Therefore, we designed,