74059-27-1

Basic information

• Product Name: N-<2-(3,4-dimethoxyphenyl)ethyl>glutarimide
• Synonyms: N-<2-(3,4-dimethoxyphenyl)ethyl>glutarimide
• CAS NO: 74059-27-1
• Molecular Weight: 277.32
• Mol File: 74059-27-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-<2-(3,4-dimethoxyphenyl)ethyl>glutarimide(CAS DataBase Reference)
• NIST Chemistry Reference: N-<2-(3,4-dimethoxyphenyl)ethyl>glutarimide(74059-27-1)
• EPA Substance Registry System: N-<2-(3,4-dimethoxyphenyl)ethyl>glutarimide(74059-27-1)

Safety Data

• Hazardous Substances Data: 74059-27-1(Hazardous Substances Data)

Upstream product

• 1121-89-7 piperidine-2,6-dione 
• 40173-90-8 3,4-dimethoxyphenethyl bromide 
• 93992-67-7 N-(3,4-dimethoxy-phenethyl)-glutaramic acid ethyl ester 
• 108-55-4 glutaric anhydride, 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 

Downstream Products

• 1371578-85-6 C₁₆H₂₃NO₄ 
• 523-01-3 (2S,3S,11bS)-2-(6,7-Dimethoxy-3,4-dihydro-isoquinolin-1-ylmethyl)-3-ethyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinoline 
• 74059-32-8 1,2,3,6,7,11b-hexahydro-9,10-dimethoxy-3-methoxycarbonyl-3-phenylselenobenzoquinolizin-4-one 
• 910564-45-3 9,10-dimethoxy-3-phenylselanyl-1,2,3,6,7,11b-hexahydro-pyrido[2,1-a]isoquinolin-4-one 
• 910564-44-2 N-[2-(3,4-dimethoxyphenyl)ethyl]-5-oxopentanamide 
• 15889-91-5 N-<2-(3,4-dimethoxyphenyl)-ethyl>-5-hydroxypentanamide 
• 32703-29-0 N-[2-(3,4-dimethoxyphenyl)ethyl]-5-oxohexanamide 
• 182552-68-7 1-[2-(2-Iodo-4,5-dimethoxy-phenyl)-ethyl]-piperidine-2,6-dione 
• 182552-70-1 N-[2-(3,4-dimethoxyphenyl)ethyl]-5-oxononanamide 
• 74059-28-2 N-(3,4-dimethoxyphenethyl)-6-ethoxy-2-piperidone 

Relevant articles and documents

Diphenyliodonium Ion/Et3N Promoted Csp2-H Radical Phosphorylation of Enamides

This work reports a simple and efficient method for the direct phosphorylation of enamide under metal-free conditions. The P-centered radicals, derived from secondary phosphine oxides, are generated under mild reaction conditions in the presence of diphenyliodonium salt and Et3N and are introduced onto a range of enamides in good isolated yields. The method features broad substrate scope, good functional group tolerance, and efficient scale-up.

Conjugate additions of sulfur-stabilized anions to unsaturated lactams. Synthesis of polyfunctionalized benzo[a]quinolizinone systems

Conjugate addition reactions of sulfur-stabilized nucleophiles to the δ-lactam unit of tetrahydrobenzo[a]benzoquinolizines have been studied. The stereochemical outcome of the conjugate addition reaction depends on the nature of the substituent at the ang

Parham-type cyclization and nucleophilic addition-N-acyliminium ion cyclization sequences for the construction of the isoquinoline nucleus

Efficient methodologies based on the nucleophilic addition-N-acyliminium ion cyclization and the Parham-type cyclization sequences of N-phenethylimides 1 and 2 are reported for the synthesis of a dibenzo[a,h]quinolizidones, thiazolo-, oxazolo-, and imidazolo[4,3-a]isoquinolones.