10242-40-7

Basic information

• Product Name: 1,1-diethoxy-1-phenylpropane
• Synonyms: 1,1-diethoxy-1-phenylpropane
• CAS NO: 10242-40-7
• Molecular Weight: 208.301
• Mol File: 10242-40-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,1-diethoxy-1-phenylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-diethoxy-1-phenylpropane(10242-40-7)
• EPA Substance Registry System: 1,1-diethoxy-1-phenylpropane(10242-40-7)

Safety Data

• Hazardous Substances Data: 10242-40-7(Hazardous Substances Data)

Upstream product

• 673-32-5 1-Phenylprop-1-yne 
• 64-17-5 ethanol 
• 122-51-0 orthoformic acid triethyl ester 
• 93-55-0 1-phenyl-propan-1-one 

Downstream Products

• 859314-73-1 ethyl-(1-phenyl-propenyl)-ether 
• 100121-62-8 3-ethoxy-2-methyl-3-phenyl-acrylaldehyde 
• 14182-01-5 (2E)-2-methyl-1,3-diphenylprop-2-en-1-one 
• 33815-55-3 (2SR,3RS)-2-methyl-3-phenyl-2,3-dihydro-1H-inden-1-one 
• 93-55-0 1-phenyl-propan-1-one 
• 1138700-40-9 N-1-phenylpropylidene-diphenylthiophosphinamide 
• 105340-57-6 3-dimethylamino-2-methyl-3-phenyl-acrylaldehyde 
• 87876-92-4 N-(1-phenylpropyl)-N-ethylamine 
• 133100-01-3 diethyl-(1-phenyl-propyl)-amine 
• 92111-08-5 butyl-(1-phenylpropyl)amine 
• 3330-05-0 α-ethyl-N,N-dimethylbenzenemethanamine 
• 2941-20-0 1-phenylpropylamine 
• 15429-18-2 N-benzyl-α-ethylbenzylamine 
• 7713-71-5 N-methyl-1-phenylpropan-1-amine 

Relevant articles and documents

Synthesis and structures of heterobimetallic Ir2M (M=Pd, Pt) sulfido clusters and their catalytic activity for regioselective addition of alcohols to internal 1-aryl-1-alkynes

The heterobimetallic trinuclear suffido clusters [(Cp*Ir)2(μ3-S)2MCl2] (M = Pd (3), Pt (4); Cp* = η5-C5Me5) were synthesized from the dinuclear hydrogensulfido complex [Cp*IrCl(μ

Regioselective addition of alcohols to internal 1-aryl-1-alkynes catalyzed by a triangular heterobimetallic Ir2Pd sulfido cluster

The triangular heterobimetallic sulfido cluster [(Cp*Ir)2(μ3-S)2PdCl2] prepared from [PdCl2(cod)] and [Cp*IrCl(μ-SH)2IrCp*Cl] was found to catalyze the addition of alcohols to alkynes to give the corresponding ketals. In particular, internal 1-aryl-1-alkynes were transformed into the corresponding 2,2-dialkoxy-1-arylalkanes with high regioselectivity. The analogous Ir2PtS2 cluster proved to be much less selective.