Название продукции:(2-(N-(tert-Butyl)sulfamoyl)-5-isobutylthiophen-3-yl)boronic acid
IUPAC Name:[2-(tert-butylsulfamoyl)-5-(2-methylpropyl)thiophen-3-yl]boronic acid
- CAS:163520-14-7
- Молекулярная формула:C12H22BNO4S2
- Чистота:95%
- Номер в каталоге:CM210843
- Молекулярная масса:319.24
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Информация о продукции
- Номер CAS:163520-14-7
- Молекулярная формула:C12H22BNO4S2
- Точка плавления:-
- Smiles-код:CC(C)CC1=CC(B(O)O)=C(S(=O)(NC(C)(C)C)=O)S1
- Плотность:
- Номер в каталоге:CM210843
- Молекулярная масса:319.24
- Точка кипения:
- Номер Mdl:MFCD17169309
- Хранение:
Category Infos
- Thiophenes
- Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
- 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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