1-Methyl-1H-pyrazole-5-boronic acid pinacol ester

CAS: 847818-74-0

Ref. 3D-FM121885

Product Information

• Name: 1-Methyl-1H-pyrazole-5-boronic acid pinacol ester
• Synonyms: 1-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole, 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

Description

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.

• Brand: Biosynth

Chemical properties

• Molecular weight: 208.07 g/mol
• Formula: C₁₀H₁₇BN₂O₂
• Purity: Min. 95%
• InChI: InChI=1S/C10H17BN2O2/c1-9(2)10(3,4)15-11(14-9)8-6-7-12-13(8)5/h6-7H,1-5H3
• InChI key: InChIKey=HLXOVAMYQUFLPE-UHFFFAOYSA-N
• SMILES: Cn1nccc1B1OC(C)(C)C(C)(C)O1