ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Research Reagent/1-Cyclopentenylboronic acid pinacol ester
C11H19BO2
194.08 g/mol
Research ReagentWarning

2-(CYCLOPENT-1-EN-1-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE

CAS287944-10-9EC801-068-1
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

This compound is a boronic ester synthetic reagent, commonly used in organic chemistry for Suzuki-type coupling reactions. It features a cyclopentenyl group attached to a pinacol boronate ester framework.

Reagent for Suzuki-Miyaura cross-coupling reactionsBuilding block in organic synthesis

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 287944-10-9

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

StrongStructure SimilarSimilarity 0.88

Cyclohexene-1-boronic acid pinacol ester

CAS141091-37-4

research compound

ApplicationSame Use

4,4,5,5-Tetramethyl-2-[(1E)-pent-1-en-1-yl]-1,3,2-dioxaborolane

CAS161395-96-6

research compound

ReferenceSame Category

4-[4-(Trifluoromethoxy)phenoxy]piperidine

CAS287952-67-4

research compound

ReferenceSame Category

Pyrazole

CAS288-13-1

research compound

ReferenceSame Category

1,2,3-Triazole

CAS288-36-8

research compound

ReferenceSame Category

N²-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-L-α-glutamine

CAS288149-55-3

research compound

Safety Reference

Harmful
Harmful
Warning
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name

2-(cyclopenten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

InChIKey

JFTZVYKESKQING-UHFFFAOYSA-N

SMILES

B1(OC(C(O1)(C)C)(C)C)C2=CCCC2

Synonyms (10)

—