Description
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole (CAS: 937366-55-7) is a high-purity boronic ester derivative of indazole, designed for advanced synthetic and medicinal chemistry applications. With the molecular formula C13H17BN2O2, this compound features a stable pinacol boronate group, making it an essential reagent for Suzuki-Miyaura cross-coupling reactions and other boron-mediated transformations. Ideal for researchers and pharmaceutical developers, this product is rigorously tested for consistency, purity (>95%), and performance in complex organic syntheses. Its crystalline solid form ensures easy handling and precise dosing in laboratory settings. Packaged under inert conditions to maintain stability, it is a critical building block for drug discovery, agrochemical research, and material science applications.
Properties
- CAS Number: 937366-55-7
- Complexity: 319
- IUPAC Name: 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
- InChI: InChI=1S/C13H17BN2O2/c1-12(2)13(3,4)18-14(17-12)11-9-7-5-6-8-10(9)15-16-11/h5-8H,1-4H3,(H,15,16)
- InChI Key: UWAAHKNOJPKHNF-UHFFFAOYSA-N
- Exact Mass: 244.1383080
- Molecular Formula: C13H17BN2O2
- Molecular Weight: 244.10
- SMILES: B1(OC(C(O1)(C)C)(C)C)C2=C3C=CC=CC3=NN2
- Topological: 47.1
- Monoisotopic Mass: 244.1383080
- Synonyms: 937366-55-7, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1h-indazole, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole, MFCD07368014, 1607787-21-2, 1H-Indazole-3-boronic acid pinacol ester, SCHEMBL1104787, SCHEMBL15504185, DTXSID60695719, UWAAHKNOJPKHNF-UHFFFAOYSA-N, indazole boronic acid pinacol ester, 3-Indazoleboronic Acid Pinacol Ester, AKOS025293845, AT16497, MB04416, BS-29787, SY279723
This compound is widely used as a key intermediate in the synthesis of biologically active molecules, particularly in pharmaceutical research for kinase inhibitors and anticancer agents. Its boronic ester functionality enables efficient cross-coupling reactions to construct heterocyclic scaffolds. Suitable for high-throughput screening and combinatorial chemistry due to its stability and reactivity. Also employed in the development of fluorescent probes and sensors for biochemical studies.
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