13125-59-2

Basic information

• Product Name: Benzenemethanol, a-(2-methoxyethyl)-
• Synonyms: 3-Methoxy-1-phenyl-1-propanol
• CAS NO: 13125-59-2
• Molecular Formula: C10H14O2
• Molecular Weight: 166.22
• Mol File: 13125-59-2.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 113-125 °C(Press: 12 Torr)
• Density: 1.0460 g/cm3
• CAS DataBase Reference: Benzenemethanol, a-(2-methoxyethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(2-methoxyethyl)-(13125-59-2)
• EPA Substance Registry System: Benzenemethanol, a-(2-methoxyethyl)-(13125-59-2)

Safety Data

• Hazardous Substances Data: 13125-59-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 873-49-4 cyclopropylbenzene 
• 55955-55-0 methyl 3-chloro-3-phenylpropyl ether 
• 772-00-9 4-phenyl-1,3-dioxane 
• 16277-67-1 3-methoxy-1-phenylpropene 
• 40685-20-9 (E)-3-methoxy-1-phenylprop-2-en-1-one 
• 100-42-5 styrene 
• 98-88-4 benzoyl chloride 
• 127618-32-0 2-Diazo-3-methoxy-1-phenylpropanone 
• 55563-72-9 3-methoxy-1-phenylpropan-1-one 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 

Downstream Products

• 18344-98-4 1-<β-Amino-aethoxy>-1-phenyl-3-methoxy-propan 
• 18344-97-3 1--1-phenyl-3-methoxy-propan 
• 18344-96-2 1-Phenyl-1-<β-cyan-aethoxy>-3-methoxy-propan 
• 26278-67-1 1,3-dimethoxy-1-phenylpropane 
• 1605319-69-4 1-azido-3-methoxy-1-phenylpropane 
• 55563-71-8 Ethyl(2-methoxyethyl)phenylmethanol 
• 137040-14-3 2-Hydroxy-4-methoxy-2-phenyl-butyric acid 1-aza-bicyclo[2.2.2]oct-3-yl ester 
• 137039-86-2 4-Methoxy-2-phenyl-2-trimethylsilanyloxy-butyronitrile 
• 137040-07-4 2-Hydroxy-4-methoxy-2-phenyl-butyric acid ethyl ester 
• 137039-93-1 2-Hydroxy-4-methoxy-2-phenyl-butyramide 
• 137040-00-7 2-Hydroxy-4-methoxy-2-phenyl-butyric acid 
• 88241-49-0 8-methoxy-4-methyl-6-phenyl-3-(1'-phenylcyclopropyl)(2,4,5-D₃)octa-2,5-diene 
• 79012-25-2 8-methoxy-4-methyl-6-phenyl-3-(1'-phenylcyclopropyl)octa-2,5-diene 
• 88241-50-3 (4-D)(E)-1-methoxy-3-phenylhex-4-en-3-ol 

Relevant articles and documents

Pentacoordinate vs. Tetracoordinate complexation for alkoxycarbonyl compounds with dialkylboron triflates and trifluoroacetates?

The implication of hitherto unknown pentacoordinate complex formation for alkoxycarbonyl compounds with Et2BX (X =OTf, OCOCF3) is presented by several reduction/allylation experiments and low-temperature 13C, 11

Cobalt(II) Porphyrin-Catalyzed Oxidation of Olefins to Ketones with Molecular Oxygen and Triethylsilane in 2-Propanol

An efficient conversion of olefins to ketones was achieved by the use of molecular oxygen and triethylsilane in the presence of a catalytic amount of cobalt(II) complex of porphyrin.The oxidation was accelerated remarkably in alcohols and had chomoselectivity for conjugated olefins.