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| IUPAC Name: | 1,3-benzodioxol-5-ylboronic acid |
| Description: | Reactant involved in: Petasis reaction between glyoxylic acid, α-amino phosphonates, and organylboronic acids; Mannich-type multicomponent assembly and 1,3-dipolar cycloaddition for synthesis of tetrahydroisoquinoline fused isoxazolidine scafford; Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides; Oxidative Heck reaction for synthesis of functionalized cinnamaldehyde derivatives; Intramolecular Alder-ene and Pictet-Spengler reactions for synthesis of crinine. |
| Molecular Weight: | 165.94 |
| Molecular Formula: | C7H7O4B |
| Canonical SMILES: | B(C1=CC2=C(C=C1)OCO2)(O)O |
| InChI: | InChI=1S/C7H7BO4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3,9-10H,4H2 |
| InChI Key: | CMHPUBKZZPSUIQ-UHFFFAOYSA-N |
| Boiling Point: | 347.342 ℃ at 760 mmHg |
| Melting Point: | 224-229 ℃ (lit.) |
| Flash Point: | Not applicable |
| Purity: | ≥ 95 % |
| Density: | 1.423 g/cm3 |
| Storage: | Keep in dark place, Sealed in dry, Room Temperature |
| MDL: | MFCD01009695 |
| LogP: | -0.90490 |
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