842150-42-9

Basic information

• Product Name: Silane, (1,1-dimethylethyl)[4-(1,3-dioxan-2-yl)-2-methoxyphenoxy]dimethyl-
• CAS NO: 842150-42-9
• Molecular Formula: C17H28O4Si
• Molecular Weight: 324.492
• Mol File: 842150-42-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Silane, (1,1-dimethylethyl)[4-(1,3-dioxan-2-yl)-2-methoxyphenoxy]dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, (1,1-dimethylethyl)[4-(1,3-dioxan-2-yl)-2-methoxyphenoxy]dimethyl-(842150-42-9)
• EPA Substance Registry System: Silane, (1,1-dimethylethyl)[4-(1,3-dioxan-2-yl)-2-methoxyphenoxy]dimethyl-(842150-42-9)

Safety Data

• Hazardous Substances Data: 842150-42-9(Hazardous Substances Data)

Upstream product

• 69404-94-0 O-tert-butyldimethylsilylvanillin 
• 504-63-2 trimethyleneglycol 
• 121-33-5 vanillin 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 842150-47-4 methyl 7-benzyloxy-6-iodo-8-methoxy-1-oxo-1H-isochromene-3-carboxylate 
• 842150-44-1 methyl 6-formyl-3-hydroxy-4-iodo-2-methoxybenzoate 
• 842150-43-0 methyl 6-formyl-3-hydroxy-2-methoxybenzoate 
• 877662-87-8 methyl (E)-3-benzyloxy-4-iodo-2-methoxy-6-(2-methoxycarbonyl-2-tert-butyldimethylsiloxyethynyl)benzoate 
• 877662-88-9 6-benzyloxy-3-hydroxy-5-iodo-7-methoxy-3H-benzofuran-1-one 
• 877662-86-7 methyl 3-benzyloxy-6-formyl-4-iodo-2-methoxybenzoate 
• 877662-85-6 methyl 3-(tert-butyldimethylsiloxy)-6-[(1,3)dioxan-2-yl]-2-methoxybenzoate 

Relevant articles and documents

An expedient and short synthesis of a 6-iodo isocoumarin building block for the rubromycin family and its first palladium-catalyzed couplings

An efficient six-step synthesis of 6-iodo substituted isocoumarin 6 is presented, which is a suitable building block for the preparation of rubromycin type compounds. Key transformations of the sequence were achieved by directed ortho-lithiation, Horner-W

Towards the rubromycins: An efficient synthesis of a suitable isocoumarin precursor, its lactam analogue, and palladium-catalyzed couplings

6-Iodoisocoumarin 4 and its aza-analogue, 6-iodo-1-oxo-isoquinoline 29, were efficiently prepared from vanillin in seven and six steps, respectively. Key transformations in their syntheses were achieved by directed ortho-lithiation and variations of Horne