1572927-00-4

Basic information

• Product Name: 2-([1,1'-biphenyl]-4-yl)-N-benzyl-N-methylacetamide
• Synonyms: 2-([1,1'-biphenyl]-4-yl)-N-benzyl-N-methylacetamide
• CAS NO: 1572927-00-4
• Molecular Weight: 315.415
• Mol File: 1572927-00-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-([1,1'-biphenyl]-4-yl)-N-benzyl-N-methylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-([1,1'-biphenyl]-4-yl)-N-benzyl-N-methylacetamide(1572927-00-4)
• EPA Substance Registry System: 2-([1,1'-biphenyl]-4-yl)-N-benzyl-N-methylacetamide(1572927-00-4)

Safety Data

• Hazardous Substances Data: 1572927-00-4(Hazardous Substances Data)

Upstream product

• 29079-00-3 4-ethynyl-1,1'-biphenyl 
• 103-67-3 benzyl-methyl-amine 
• 5728-52-9 (4-biphenylyl)acetic acid 

Relevant articles and documents

Oxidation of Alkynyl Boronates to Carboxylic Acids, Esters, and Amides

A general efficient protocol was developed for the synthesis of carboxylic acids, esters, and amides through oxidation of alkynyl boronates, generated directly from terminal alkynes. This protocol represents the first example of C(sp)?B bond oxidation. This approach displays a broad substrate scope, including aryl and alkyl alkynes, and exhibits excellent functional group tolerance. Water, primary and secondary alcohols, and amines are suitable nucleophiles for this transformation. Notably, amino acids and peptides can be used as nucleophiles, providing an efficient method for the synthesis and modification of peptides. The practicability of this methodology was further highlighted by the preparation of pharmaceutical molecules.