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Tavaborole

SIGMA/SML1227 - ≥95% (HPLC)

Synonym: 1,3-Dihydro-5-fluoro-1-hydroxy-2,1-benzoxaborole; 5-Fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole; AN-2690; AN2690

CAS Number: 174671-46-6
Empirical Formula (Hill Notation): C7H6BFO2
Molecular Weight: 151.93
Linear Formula: C7H6BFO2
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-SML1227-10MG 10 mg
 $127.00
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45-SML1227-50MG 50 mg
 $475.00
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This image is provided for informative purposes only and does not represent an actual product label. It should not be used as a substitute for official product labeling.

 

assay ≥95% (HPLC)
color white to beige
form powder
InChI 1S/C7H6BFO2/c9-6-1-2-7-5(3-6)4-11-8(7)10/h1-3,10H,4H2
InChI key LFQDNHWZDQTITF-UHFFFAOYSA-N
Quality Level 100 
SMILES string B1(OCc2c1ccc(c2)F)O
solubility DMSO: 20 mg/mL, clear
storage condition desiccated
storage temp. −20°C
Biochem/physiol Actions: Tavaborole (AN2690) is a potent antifungal that targets the post-transfer editing site of leucyl-tRNA synthetase (LeuRS).
Biochem/physiol Actions: Tavaborole (AN2690) is a potent antifungal that targets the post-transfer editing site of leucyl-tRNA synthetase (LeuRS). Tavaborole forms a covalent adduct with the 3′ adenosine of tRNA(leu) at the editing site of fungal, but not bacterial LeuRS, locking the enzyme in an inactive conformation. Tavaborole was recently approved for the treatment of onychomycosis of the toenail in adults.
General description: Tavaborole is a boron-based pharmaceutical agent. It has broad-spectrum oxaborole antifungal activity. Due to its low molecular weight, it facilitates maximal nail plate penetration than its predecessors.
Packaging: 10, 50 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95% (HPLC)
Storage Temp. −20°C
UNSPSC 12352200

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