6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol

Name: 6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol
Brand: ChemScene
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CAS No. 174671-89-7
Cat. No. CS-0078611
Molecule weight151.93
Purity≥98%
MDL No.MFCD10699481

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Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

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6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol|CS-0078611

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General Information

CAS No. 174671-89-7
Cat. No. CS-0078611
Purity ≥98%
MDL No. MFCD10699481
Storage Store at room temperature
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₇H₆BFO₂
Molecular Weight 151.93
Synonym(s) 6-Fluoro-1-hydroxyl-1,3-dihydrobenzo[c][1,2]oxaborole
SMILES OB1C2=CC(F)=CC=C2CO1

Description

6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol features a boronate moiety fused to a fluorinated benzene ring, combining enhanced stability with high reactivity in cross-coupling processes. The electron-withdrawing fluorine substituent modulates boron electrophilicity, enabling efficient palladium-catalyzed transformations under mild conditions. This bench-stable scaffold integrates readily into complex molecular architectures.

Application

6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its fluorinated aryl core enhances metabolic stability and modulates electronic properties, enabling efficient C–C bond formation under mild conditions. The oxaborolone scaffold exhibits excellent functional group tolerance and compatibility with diverse reaction partners, facilitating the synthesis of complex biaryl architectures relevant to pharmaceutical development.

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

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Computational Chemistry Data

TPSA 29.46
LogP 0.0434
H_Acceptors 2
H_Donors 1
Rotatable_Bonds 0

Other Classifications

Building Blocks Functional Group Boronic Acid And Its Ester

Building Blocks Skeleton Aromatic heterocycle compounds Other aromatic heterocycles compounds

Key Words

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6-Fluorobenzo[c][1,2]oxaborol-1(3H)-ol

CAS No. 174671-89-7

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