34059-10-4

Basic information

• Product Name: N-(3-Phenylpropyl)acetamide
• Synonyms: N-(3-Phenylpropyl)acetamide
• CAS NO: 34059-10-4
• Molecular Formula: C₁₁H₁₅NO
• Molecular Weight: 177.24
• Mol File: 34059-10-4.mol
• Article Data: 23

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(3-Phenylpropyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-Phenylpropyl)acetamide(34059-10-4)
• EPA Substance Registry System: N-(3-Phenylpropyl)acetamide(34059-10-4)

Safety Data

• Hazardous Substances Data: 34059-10-4(Hazardous Substances Data)

Upstream product

• 27129-74-4 N-nitroso-N-(3-phenyl-propyl)-acetamide 
• 2038-57-5 3-Phenylpropan-1-amine 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 
• 506-96-7 Acetyl bromide 
• 75-16-1 methylmagnesium bromide 
• 111944-09-3 methyl N-(3-phenylpropyl)carbamate 
• 302569-84-2 N-benzyloxycarbonyloxy-3-phenylpropylamine 
• 122-97-4 3-Phenyl-1-propanol 
• 75-05-8 acetonitrile 
• 108-22-5 Isopropenyl acetate 
• 60-35-5 acetamide 
• 100-42-5 styrene 
• 201230-82-2 carbon monoxide 

Downstream Products

• 27129-74-4 N-nitroso-N-(3-phenyl-propyl)-acetamide 
• 13125-62-7 1-(ethylamino)-3-phenylpropane 
• 58347-62-9 N-[3-(4-Butyryl-phenyl)-propyl]-acetamide 
• 53199-94-3 4-[3-(acetylamino)propyl]benzenesulfonyl chloride 
• 374632-74-3 4-[3-(acetylamino)propyl]-N-(2-phenyl-2H-pyrazol-3-yl)benzenesulfonamide 
• 693789-98-9 benzoic acid 3-[[4-(3-acetylamino-propyl)-benzenesulfonyl]-(2-phenyl-2H-pyrazol-3-yl)-amino]-propyl ester 
• 287174-96-3 N-{3-[4-(4-chloro-butyl)-phenyl]-propyl}-acetamide 
• 58347-63-0 3-(4'-Butylphenyl)propylamin 
• 58347-65-2 [3-(4-Butyl-phenyl)-propyl]-methyl-amine 
• 58347-64-1 N-[3-(4-Butyl-phenyl)-propyl]-formamide 
• 223512-49-0 N-(3-(2-formylphenyl)propyl)acetamide 
• 1329563-45-2 N-{3-[4-(5-chloropentanoyl)phenyl]propyl}acetamide 
• 1329563-34-9 N-{3-[4-(5-chloropentyl)phenyl]propyl}acetamide 
• 1329563-27-0 {3-[4-(3-chloropropyl)phenyl]propyl}ethylamine 

Relevant articles and documents

Hydrosilylative reduction of primary amides to primary amines catalyzed by a terminal [Ni-OH] complex

A terminal [Ni-OH] complex1, supported by triflamide-functionalized NHC ligands, catalyzes the hydrosilylative reduction of a range of primary amides into primary amines in good to excellent yields under base-free conditions with key functional group tolerance. Catalyst1is also effective for the reduction of a variety of tertiary and secondary amides. In contrast to literature reports, the reactivity of1towards amide reduction follows an inverse trend,i.e., 1° amide > 3° amide > 2° amide. The reaction does not follow a usual dehydration pathway.

Direct Intermolecular Anti-Markovnikov Hydroazidation of Unactivated Olefins

We herein report a direct intermolecular anti-Markovnikov hydroazidation method for unactivated olefins, which is promoted by a catalytic amount of bench-stable benziodoxole at ambient temperature. This method facilitates previously difficult, direct addition of hydrazoic acid across a wide variety of unactivated olefins in both complex molecules and unfunctionalized commodity chemicals. It conveniently fills a synthetic chemistry gap of existing olefin hydroazidation procedures, and thereby provides a valuable tool for azido-group labeling in organic synthesis and chemical biology studies.

Bis-arylalkenylalkyl acid compound, and preparation method and application thereof

The invention relates to a bis-arylalkenylalkyl acid compound, and a preparation method and an application thereof. The structure of the compound is represented by the formula I. the definitions of *, R1, R2, R3, n1 and m are as in the specifications and the claims. The bis-arylalkenylalkyl acid compound provided by the invention has relatively high inhibition activity against sensitive strains and resistant strains, and can be used for preparing antibacterial drugs.