20330-65-8

Basic information

• Product Name: N-(4-heptylphenyl)acetamide
• Synonyms: N-(4-heptylphenyl)acetamide
• CAS NO: 20330-65-8
• Molecular Formula: C₁₅H₂₃NO
• Molecular Weight: 233.34922
• Mol File: 20330-65-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-heptylphenyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-heptylphenyl)acetamide(20330-65-8)
• EPA Substance Registry System: N-(4-heptylphenyl)acetamide(20330-65-8)

Safety Data

• Hazardous Substances Data: 20330-65-8(Hazardous Substances Data)

Upstream product

• 37529-27-4 4-heptylaniline 
• 75-36-5 acetyl chloride 
• 628-71-7 1-Heptyne 
• 5411-50-7 3,4-dibromonitrobenzene 
• 4282-40-0 1-Iodoheptane 
• 62-53-3 aniline 
• 592-41-6 1-hexene 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 3007-70-3 N-(heptyl)aniline 
• 121866-20-4 1-(2-bromo-4-nitrophenyl)heptyne 

Relevant articles and documents

Rates and Regioselectivities of the Palladium-Catalyzed Ethynylation of Substituted Bromo- and Dibromobenzenes

The Pd(0)/Cu2Br2-catalyzed ethynylation of 1,2-dibromo-4-nitro- and 1,2-dibromo-3-nitrobenzenes provide rapidly the product in which the bromine para or ortho to the nitro group is displaced, whereas the corresponding dibromoacetamidobenzenes provide the product of meta displacement slowly.Investigation of the rates of a series of para-substituted bromobenzenes indicates that the reaction is zero-order with respect to the heptyne and bromobenzene concentration, with a Hammett ρ value of 2.8.

Study of the Influence of Molecular Length on the Characteristics of the Ordered Smectic Phase.

Study of DTA and X-rays of p-phenyl-benzylidene-p'-alkylanilines of mesomorphic phases demonstrates the predominant role of the aliphatic chain length. In effect, it governs the appearance of the different phases; the correlation between layers decreases for greater chain lengths. The nonlinear variations of SmB layer thickness for these compounds shows clearly the importance of steric effects coupled with the molecular length with respect to the dipolar effect.