Название продукции:(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate
IUPAC Name:methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propanoate
- CAS:220587-29-1
- Молекулярная формула:C21H32BNO6
- Чистота:95%
- Номер в каталоге:CM104998
- Молекулярная масса:405.3
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Информация о продукции
- Номер CAS:220587-29-1
- Молекулярная формула:C21H32BNO6
- Точка плавления:-
- Smiles-код:COC(=O)[C@H](CC1=CC=C(C=C1)B1OC(C)(C)C(C)(C)O1)NC(=O)OC(C)(C)C
- Плотность:
- Номер в каталоге:CM104998
- Молекулярная масса:405.3
- Точка кипения:
- Номер Mdl:MFCD16251714
- 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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