C5H4BNO2S
152.97 g/mol
Research ReagentDanger
5-Cyanothiophene-2-boronic acid
CAS305832-67-1EC608-502-7
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
5-Cyanothiophene-2-boronic acid is a boronic acid research reagent featuring a thiophene ring with a nitrile substituent. It is commonly used in organic synthesis and laboratory research for constructing carbon-carbon bonds via cross-coupling reactions.
research reagent in organic synthesisbuilding block for Suzuki-Miyaura coupling reactions
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.
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CAS 305832-67-1
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Safety Reference
Danger
H301Toxic if swallowed
H302Harmful if swallowed
H311Toxic in contact with skin
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H331Toxic if inhaled
H332Harmful if inhaled
H335May cause respiratory irritation
Identifiers
IUPAC Name
(5-cyanothiophen-2-yl)boronic acid
InChIKey
ZEOMEPSYIIQIND-UHFFFAOYSA-N
SMILES
B(C1=CC=C(S1)C#N)(O)O
Synonyms (8)
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