Название продукции:(S)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl-3,3'-diboronic acid pinacol ester
IUPAC Name:2-[2,2'-bis(methoxymethoxy)-3'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-binaphthalen]-3-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- CAS:260441-99-4
- Молекулярная формула:C36H44B2O8
- Чистота:95%+
- Номер в каталоге:CM573175
- Молекулярная масса:626.36
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Информация о продукции
- Номер CAS:260441-99-4
- Молекулярная формула:C36H44B2O8
- Точка плавления:-
- Smiles-код:COCOC1=C(C2=CC=CC=C2C=C1B1OC(C)(C)C(C)(C)O1)C1=C(OCOC)C(=CC2=CC=CC=C12)B1OC(C)(C)C(C)(C)O1
- Плотность:
- Номер в каталоге:CM573175
- Молекулярная масса:626.36
- Точка кипения:
- Номер Mdl:MFCD16294496
- Хранение:
Category Infos
- Boronic Acids and Esters
- Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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