Nom du produit:(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
Formule moléculaire:C12H22BNO4S2
Pureté:95%
Numéro de catalogue:CM210843
Poids moléculaire:319.24

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CM210843-100mg in stock ƥľǤ
CM210843-250mg in stock Źƿƥ
CM210843-500mg 1-2 Weeks ƓƿǤ
CM210843-1g 1-2 Weeks ƿľIJIJ

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Détails du produit

N° CAS:163520-14-7
Formule moléculaire:C12H22BNO4S2
Point de fusion:-
Code SMILES:CC(C)CC1=CC(B(O)O)=C(S(=O)(NC(C)(C)C)=O)S1
Densité:
Numéro de catalogue:CM210843
Poids moléculaire:319.24
Point d'ébullition:
N° Mdl:MFCD17169309
Stockage:

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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