63609-01-8

Basic information

• Product Name: Benzene, 4-(2-isocyanoethyl)-1,2-dimethoxy-
• CAS NO: 63609-01-8
• Molecular Formula: C11H13NO2
• Molecular Weight: 191.23
• Mol File: 63609-01-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzene, 4-(2-isocyanoethyl)-1,2-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 4-(2-isocyanoethyl)-1,2-dimethoxy-(63609-01-8)
• EPA Substance Registry System: Benzene, 4-(2-isocyanoethyl)-1,2-dimethoxy-(63609-01-8)

Safety Data

• Hazardous Substances Data: 63609-01-8(Hazardous Substances Data)

Upstream product

• 14301-36-1 N-[2-(3,4-dimethoxyphenyl)ethyl]formamide 
• 67-66-3 chloroform 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 14301-29-2 Trichlor-N-<2-(3,4-dimethoxyphenyl)ethyl>acetamid 

Downstream Products

• 1236282-90-8 2-[butyl-(5-iodo-6-methyl-2-phenylpyrimidin-4-yl)-amino]-N-[2-(3,4-dimethoxyphenyl)-ethyl]-acetamide 
• 1257212-81-9 C₂₈H₃₀N₂O₅ 
• 1357856-75-7 C₁₉H₂₃N₃O₄ 
• 1357856-77-9 C₁₈H₂₁N₃O₄ 
• 1357856-74-6 C₂₄H₂₅N₃O₄ 
• 1262152-84-0 C₁₆H₁₉N₃O₄S 
• 1262152-80-6 C₂₄H₂₁N₃O₂ 
• 1262152-20-4 C₂₄H₂₄N₄O₂ 
• 1718-87-2 8,9-dimethoxy-1-(4-methoxy-phenyl)-5,6-dihydro-imidazo[5,1-a]isoquinoline 
• 1357856-80-4 C₂₄H₂₈N₄O₄ 
• 1357856-72-4 C₂₀H₂₄N₂O₅ 
• 1262152-85-1 C₁₇H₂₁N₃O₄S 
• 1351765-16-6 N-(3,4-dimethoxyphenethyl)-2-(5-methoxy-2-(4-methoxyphenyl)-1H-benzo[d]imidazol-1-yl)-4-methylpentanamide 

Relevant articles and documents

Metal- and additive-free cascade trifluoroethylation/cyclization of organic isoselenocyanates by phenyl(2,2,2-trifluoroethyl)iodonium triflate

A novel and convenient cascade trifluoroethylation/cyclization of organic isoselenocyanates by phenyl(2,2,2-trifluoroethyl)iodonium triflate is reported. A series of 2-isoselenocyanobiaryls and aryl alkyl isoselenocyanates reacted with phenyl(2,2,2-trifluoroethyl)iodonium triflate in CH2Cl2 at 40 °C under metal- and additive-free conditions for 3 h to provide the corresponding trifluoroethylselenolated phenanthridines and 3,4-dihydroisoquinoline derivatives in good to excellent yields. The reaction represents the first general approach to access trifluoroethylselenolated phenanthridines and 3,4-dihydroisoquinolines from organic isoselenocyanates.

Iodide-Catalyzed Synthesis of Secondary Thiocarbamates from Isocyanides and Thiosulfonates

A new method for the synthesis of secondary thiocarbamates from readily available isocyanides and thiosulfonates with broad functional group tolerance is reported. The reaction proceeds under mild reaction conditions in isopropanol and is catalyzed by inexpensive sodium iodide.

Novel ultrasound-promoted parallel synthesis of trifluoroatrolactamide library via a one-pot passerini/hydrolysis reaction sequence and their fungicidal activities

An ultrasound-promoted one-pot Passerini/hydrolysis reaction sequence has been developed for the synthesis of trifluoroatrolactamide derivatives using a diverse range of trifluoroacetophenones and isonitriles in acetic acid. Parallel synthesis in a centrifuge tube using a noncontact ultrasonic cell crusher was used in this study as an efficient method for the rapid generation of combinatorial trifluoroatrolactamide libraries, and subsequent biochemical evaluation of the resulting compounds indicated that they possessed excellent broad-spectrum fungicidal activities. N-(4-chlorophenyl)-2-(4-ethylphenyl)-3,3, 3-trifluoro-2-hydroxypropanamide and N-(4-chlorophenyl)-3,3,3-trifluoro-2- hydroxy-2-(4-methoxyphenyl)propanamide, in particular, showed significant fungicidal activities against all of the fungal species tested in the current study.