6064-43-3

Basic information

• Product Name: N-[4-(dimethylamino)phenyl]ethanediamide
• CAS NO: 6064-43-3
• Molecular Formula: C₁₃H₂₄O
• Molecular Weight: 207.2291
• Mol File: 6064-43-3.mol
• Article Data: 4

Chemical Properties

• Density: 1.284g/cm³
• Refractive Index: 1.643
• CAS DataBase Reference: N-[4-(dimethylamino)phenyl]ethanediamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(dimethylamino)phenyl]ethanediamide(6064-43-3)
• EPA Substance Registry System: N-[4-(dimethylamino)phenyl]ethanediamide(6064-43-3)

Safety Data

• Hazardous Substances Data: 6064-43-3(Hazardous Substances Data)

Upstream product

• 2528-61-2 Heptanoic acid chloride 
• 931-50-0 cyclohexylmagnesium bromide 
• 111-71-7 heptanal 
• 110-83-8 cyclohexene 
• 3761-92-0 n-hexylmagnesium bromide 
• 55894-17-2 cyclo-hexyltriphenylphosphonium iodide 
• 541-41-3 chloroformic acid ethyl ester 
• 108-94-1 cyclohexanone 
• 1671-75-6 Heptanophenone 
• 2043-61-0 cyclohexanecarbaldehyde 
• 102104-33-6 1-(1-Benzenesulfinyl-1-chloro-heptyl)-cyclohexanol 
• 70872-75-2 1-chloroheptyl phenyl sulfoxide 
• 95110-74-0 2'-hexyl-2'-phenylsulfinylspiro 
• 2719-27-9 cyclohexanylcarbonyl chloride 

Downstream Products

• 73114-17-7 Phosphoric acid (E)-2-benzenesulfonyl-1-cyclohexyl-hept-1-enyl ester diethyl ester 
• 73114-14-4 2-Benzenesulfonyl-1-cyclohexyl-heptan-1-one 
• 42371-60-8 n-pentylcyclohexylacetylene 
• 138924-61-5 (E)-7-cyclohexyl-8-pentyl-8-tetradecen-7-ol 
• 94719-38-7 1-Cyclohexyl-2-phenylsulfanyl-heptan-1-one 

Relevant articles and documents

Highly Selective Hydrogenation of Aromatic Ketones and Phenols Enabled by Cyclic (Amino)(alkyl)carbene Rhodium Complexes

Air-stable Rh complexes ligated by strongly σ-donating cyclic (amino)(alkyl)carbenes (CAACs) show unique catalytic activity for the selective hydrogenation of aromatic ketones and phenols by reducing the aryl groups. The use of CAAC ligands is essential for achieving high selectivity and conversion. This method is characterized by its good compatibility with unsaturated ketones, esters, carboxylic acids, amides, and amino acids and is scalable without detriment to its efficiency.

A NOVEL SYNTHESIS OF DIALKYL KETONES AND α-SULFENYLATED CARBONYL COMPOUNDS FROM α,β-EPOXY SULFOXIDES

Treatment of α,β-epoxy sulfoides with excess sodium phenylselenide and various kinds of alkylthiolates gave dialkyl ketones and α-sulfenylated carbonyl compounds, respectively, in good yields under mild conditions.