CAS 847818-74-0: 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
Formula:C10H17BN2O2
InChI:InChI=1/C10H17BN2O2/c1-9(2)10(3,4)15-11(14-9)8-6-7-12-13(8)5/h6-7H,1-5H3
SMILES:CC1(C)C(C)(C)OB(c2ccnn2C)O1
Synonyms:- 1H-pyrazole, 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
- 1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol
- 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
- 1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
- 1-Methylpyrazole-5-Boronic Acid Pinacol Ester
Sort by
Found 5 products.
1-Methyl-1H-pyrazole-5-boronic acid, pinacol ester
CAS:1-Methyl-1H-pyrazole-5-boronic acid, pinacol esterFormula:C10H17BN2O2Purity:98+%Color and Shape: off white solidMolecular weight:208.07g/mol1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
CAS:1-Methyl-1H-pyrazole-5-boronic acid pinacol ester is a reagent that is used in the synthesis of organic compounds. It can be used to synthesize an inorganic base, such as chloride, and is also used in the synthesis of chlorobenzene derivatives. 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester has been shown to react with suzuki coupling reactions and acylation reactions. This compound can also be used for the synthesis of malonate, which is a stable isotope that can be used for cancer research or other innovative applications. 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester reacts with iodomethane to form naphthalene derivatives, which are reductive amination products.Formula:C10H17BN2O2Purity:Min. 95%Molecular weight:208.07 g/molRef: 3D-FM121885
Discontinued product1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
CAS:Purity:98.0%Color and Shape:SolidMolecular weight:208.070007324218751H-Pyrazole, 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:Formula:C10H17BN2O2Purity:97%Color and Shape:SolidMolecular weight:208.0652
