Nom du produit:4,4,5,5-tetramethyl-2-(2-methylthiophen-3-yl)-1,3,2-dioxaborolane

IUPAC Name:4,4,5,5-tetramethyl-2-(2-methylthiophen-3-yl)-1,3,2-dioxaborolane

CAS:910553-12-7
Formule moléculaire:C11H17BO2S
Pureté:95%
Numéro de catalogue:CM126363
Poids moléculaire:224.13

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CM126363-1g in stock ĜŁř
CM126363-5g in stock řřǭ
CM126363-10g 1-2 Weeks ƩĜŽƏ

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Détails du produit

N° CAS:910553-12-7
Formule moléculaire:C11H17BO2S
Point de fusion:-
Code SMILES:CC1=C(B2OC(C)(C)C(C)(C)O2)C=CS1
Densité:
Numéro de catalogue:CM126363
Poids moléculaire:224.13
Point d'ébullition:
N° Mdl:MFCD09837623
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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