3532-58-9

Basic information

• Product Name: 1-phenyl-2-nitroethyl methyl ether
• Synonyms: 1-phenyl-2-nitroethyl methyl ether
• CAS NO: 3532-58-9
• Molecular Weight: 181.191
• Mol File: 3532-58-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-phenyl-2-nitroethyl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-2-nitroethyl methyl ether(3532-58-9)
• EPA Substance Registry System: 1-phenyl-2-nitroethyl methyl ether(3532-58-9)

Safety Data

• Hazardous Substances Data: 3532-58-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 102-96-5 (2-nitroethenyl)benzene 
• 3532-83-0 2-nitro-1-nitrosoethylbenzene 
• 124-41-4 sodium methylate 
• 5153-67-3 nitrostyrene 
• 100-42-5 styrene 

Downstream Products

• 3490-79-7 2-methoxy-2-phenylethan-1-amine 
• 858011-45-7 N-(β-methoxy-phenethyl)-phthalamic acid methyl ester 
• 858011-46-8 N-(β-methoxy-phenethyl)-phthalamic acid 
• 23092-87-7 2-[(E)-2-phenylvinyl]-1H-isoindole-1,3(2H)-dione 

Relevant articles and documents

On-water magnetic NiFe2O4 nanoparticle-catalyzed Michael additions of active methylene compounds, aromatic/aliphatic amines, alcohols and thiols to conjugated alkenes

Here, we have demonstrated the Michael addition of active methylene compounds, aromatic/aliphatic amines, thiols and alcohols to conjugated alkenes using magnetic nano-NiFe2O4 as reusable catalyst in water. Nano-NiFe2O4 efficiently catalyzed the formation of C-C and C-X (X = N, S, O etc.) bond through 1,4-addition reactions.

β-Alkoxy-substituted phenethylamines: A family of compounds potentially active at the dopamine and α-adrenergic receptors

A series of β-alkoxy-substituted phenethylamines were synthesized and tested for their affinity at the D1 and D2 dopaminergic receptors and the α1 and α2 adrenoceptors. None of the tested compounds exhibited D2 receptor af