6907-74-0

Upstream product

• 107-10-8 propylamine 
• 536-74-3 phenylacetylene 
• 98-86-2 acetophenone 

Downstream Products

• 450-95-3 2-fluoroacetophenone 
• 395-01-7 2,2-difluoro-1-phenylethanone 
• 1588764-85-5 (Z)-3-phenyl-3-propylaminoprop-2-enethioic acid N-(4-chlorophenyl)amide 
• 1588764-87-7 C₁₈H₁₉FN₂S 
• 19302-30-8 (S)-N-(1-phenylethyl)-propan-1-amine 
• 66896-60-4 N-(1-phenylethyl)propan-1-amine 

Relevant academic research and scientific papers

Ancillary ligand-free copper catalysed hydrohydrazination of terminal alkynes with NH2NH2

An efficient and selective Cu-catalysed hydrohydrazination of terminal alkynes with parent hydrazine is reported. The methodology tolerates a broad range of functional groups, allows for the synthesis of symmetrical and unsymmetrical azines, and can be extended to hydrazine derivatives and amines.

Synthesis of 2,5-dihydroisothiazole derivatives. 2*. 3-aryl(hetaryl)-substituted 2-alkyl-5-arylimino-2,5-dihydroisothiazoles

A series of new 2-alkyl-5-arylimino-2,5-dihydroisothiazoles, substituted at position 3 with aryl and hetaryl groups and not substituted at position 4 was prepared by oxidative cyclization of N-arylamides of 3-alkylaminoprop-2- enethioic acids. The formation of the starting thioanilides was investigated by reacting the respective N-alkylimines of acetophenones with isothiocyanates. The main by-products were identified and characterized.

Polyoxyalkylene compound and method for making

A process for forming a conjugate of a polyoxyalkylene polymer (such as polyethylene glycol) with a compound containing an amine group(s) and/or a sulfide group(s) by reacting the compound with an acrylate terminated polyoxyalkylene (such as polyethylene

N-Fluoro-bis[(trifluoromethyl)sulfonyl]imide: Electrophilic fluorination of imines and some methyl-substituted pyridines

Direct fluorination of imines with N-fluoro-bis[(trifluoromethyl)sulfonyl]imide 1 afforded mono and/or difluoroketones without the need of a strong base to first generate the imine anions. Structurally related 2- and 4-methyl-substituted pyridines gave the respective fluoromethyl pyridines with 1. Our results suggest that an enamine intermediate plays a key role in these reactions.

Alkynylmercury Chloride or Acetate as Intermediates in the Mercury(II) Salt-promoted Addition of Aliphatic and Aromatic Amines to Terminal Acetylenes

Arylaminomercuriation of terminal acetylenes has been carried out with aliphatic amines to yield amines and enamines.Phenylethynylmercury chloride is shown to be an intermediate in the mercury(II) salt-promoted addition of aliphatic and aromatic amines to terminal alkynes.