C10H15BO2S
210.11 g/mol
Research ReagentWarning
4,4,5,5-tetramethyl-2-(thiophen-3-yl)-1,3,2-dioxaborolane
CAS214360-70-0EC674-923-8
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
This compound is a boronic ester used as a reagent in cross-coupling reactions. It features a thiophene ring and is commonly employed in organic synthesis and medicinal chemistry research.
Cross-coupling reagent in organic synthesisBuilding block for pharmaceutical research
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
Sourcing or supplying this compound?
List your inventory or post a purchase request
CAS 214360-70-0
Related Compounds
ApplicationSame Use
Naphthalene-2-boronic acid pinacol ester
CAS256652-04-7
research compound
ReferenceSame Category
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
CAS214360-76-6
research compound
ReferenceSame Category
2,3,4-Trihydroxybenzaldehyde
CAS2144-08-3
research compound
ReferenceSame Category
6-(pentafluoro-sulfanyl)pyridin-3-ol
CAS2144478-34-0
research compound
ReferenceSame Category
Magnesium bromide 2,6-dimethylbenzen-1-ide (1/1/1)
CAS21450-64-6
research compound
Safety Reference
Warning
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H332Harmful if inhaled
H335May cause respiratory irritation
Identifiers
IUPAC Name
4,4,5,5-tetramethyl-2-thiophen-3-yl-1,3,2-dioxaborolane
InChIKey
HQXQOBAEDQBINI-UHFFFAOYSA-N
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CSC=C2
Synonyms (7)
—