C10H19BO2
182.07 g/mol
Research ReagentWarning
4,4,5,5-Tetramethyl-2-(2-methylprop-1-en-1-yl)-1,3,2-dioxaborolane
CAS126689-00-7EC801-924-4
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound
This compound is a boronic ester commonly used as a reagent in Suzuki coupling reactions. It contains a dioxaborolane ring and an isobutenyl substituent, with no hydrogen bond donors and moderate lipophilicity.
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 126689-00-7
Related Compounds
ApplicationSame Use
3-Pyridineboronic acid pinacol ester
CAS329214-79-1
research compound
ApplicationSame Use
5-Chlorothiophene-2-boronic acid pinacol ester
CAS635305-24-7
research compound
ApplicationSame Use
2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS1012084-56-8
research compound
ApplicationSame Use
3-Methoxy-5-pyridineboronic acid pinacol ester
CAS445264-60-8
research compound
ReferenceSame Category
4-(1,3,2-Dioxaborinan-2-yl)benzoic acid
CAS126747-13-5
research compound
ReferenceSame Category
4-Cyanophenylboronic acid
CAS126747-14-6
research compound
ReferenceSame Category
7-Bromo-4-chloro-1H-indole
CAS126811-29-8
research compound
ReferenceSame Category
7-bromo-2-phenyl-Benzoxazole
CAS1268137-13-8
research compound
Safety Reference
Warning
H227
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
4,4,5,5-tetramethyl-2-(2-methylprop-1-enyl)-1,3,2-dioxaborolane
InChIKey
LWXHOCHDERDUID-UHFFFAOYSA-N
SMILES
B1(OC(C(O1)(C)C)(C)C)C=C(C)C
Synonyms (10)
—