1-(Tetrahydropyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester
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1-(Tetrahydropyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester

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1-(Tetrahydropyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester can be used as a reactant in Suzuki coupling reaction for the preparation of heteroaryl scaffolds via formation of C-C bond and to synthesize darolutamide derivatives as potential androgen receptor inhibitors.

Category
Peptide Synthesis Reagents
Catalog number
BAT-006320
CAS number
903550-26-5
Molecular Formula
C14H23BN2O3
Molecular Weight
278.15
1-(Tetrahydropyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester
IUPAC Name
1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
Synonyms
1-(Tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole; 1-(2-Tetrahydropyranyl)-1H-Pyrazole-5-Boronic acid pinacol ester; 1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazole-5-boronic acid pinacol ester; MFCD09037501; 1-(oxan-2-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole; 1-(Oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole; 1-THP-1H-PYRAZOLYL-5-BORONIC ACID PINACOL ESTER; 1-(2-Tetrahydropyranyl)pyrazole-5-boronic Acid Pinacol Ester; 1-(2-Tetrahydropyranyl)-1H-pyrazole-5-boronic acid pinacol ester; 1-THP-1H-Pyrazolyl-5-boronic acid pinacol ester; 1-(TETRAHYDROPYRAN-2-YL)-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRAZOLE; 2-(1-(2H-3,4,5,6-tetrahydropyran-2-yl)pyrazol-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; PubChem18442; ACMC-209ygx; AMTB162; KSC915I9P; SCHEMBL365094
Appearance
White to quasi-white powder
Purity
> 98 % (GC)
Density
1.160±0.10 g/cm3 (Predicted)
Melting Point
74-78 °C
Boiling Point
413.8±35.0 °C (Predicted)
Storage
2-8 °C
InChI
InChI=1S/C14H23BN2O3/c1-13(2)14(3,4)20-15(19-13)11-8-9-16-17(11)12-7-5-6-10-18-12/h8-9,12H,5-7,10H2,1-4H3
InChI Key
ZZRFDLHBMBHJTI-UHFFFAOYSA-N
Canonical SMILES
B1(OC(C(O1)(C)C)(C)C)C2=CC=NN2C3CCCCO3
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