142592-52-7

Basic information

• Product Name: Benzoic acid, 5-(phenylmethoxy)-2-[[2-(trimethylsilyl)ethoxy]methoxy]-, methyl ester
• CAS NO: 142592-52-7
• Molecular Formula: C21H28O5Si
• Molecular Weight: 388.536
• Mol File: 142592-52-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 5-(phenylmethoxy)-2-[[2-(trimethylsilyl)ethoxy]methoxy]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 5-(phenylmethoxy)-2-[[2-(trimethylsilyl)ethoxy]methoxy]-, methyl ester(142592-52-7)
• EPA Substance Registry System: Benzoic acid, 5-(phenylmethoxy)-2-[[2-(trimethylsilyl)ethoxy]methoxy]-, methyl ester(142592-52-7)

Safety Data

• Hazardous Substances Data: 142592-52-7(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 2150-46-1 Methyl 2,5-dihydroxybenzoate 
• 61227-22-3 methyl 2-hydroxy-5-(phenylmethoxy)benzoate 
• 76513-69-4 (2-trimethylethylsilylethoxy)methyl chloride 

Downstream Products

• 142592-60-7 <2S(S),3R,6S,8S>-N-<6-hydroxy-2-(methoxycarbonyl)-3-<<2-(trimethylsilyl)ethoxy>methoxy>phenyl>-2-<1-<<1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-pyrrolidyl>carbonyl>ethyl>-1,7-dioxaspiro<5.5>undecane-8-acetamide 
• 99623-84-4 Routiennocin 
• 144604-76-2 N-<6-hydroxy-2-(methoxycarbonyl)-3-<<2-(trimethylsilyl)ethoxy>methoxy>phenyl> benzenepropanamide 
• 142592-54-9 methyl 5-oxo-4-<(phenylselenyl)imino>-2-<<2-(trimethylsilyl)ethoxy>methoxy>-1,3-cyclohexadienecarboxylate 
• 142592-55-0 methyl 5-oxo-6-<(phenylselenyl)imino>-2-<<2-(trimethylsilyl)ethoxy>methoxy>-1,3-cyclohexadienecarboxylate 
• 144604-77-3 methyl 5-hydroxy-2-(2-phenethyl)-4-benzoxazolecarboxylate 
• 142592-43-6 methyl 2-amino-3-hydroxy-6-<<2-(trimethylsilyl)ethoxy>methoxy> benzoate 
• 142592-53-8 methyl 2-<<2-(trimethylsilyl)ethoxy>methoxy>-5-hydroxy benzoate 

Relevant articles and documents

Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin)

The total synthesis of the spiroketal ionophore antibiotic routiennocin 1 (CP-61,405) employing π-allyltricarbonyl iron lactone complexes is described. These complexes were used as precursors for the preparation of substituted 2-phenylsulphonyl pyrans whi