Other grades of this product :
| 2-Tolylboronic acid Chemical Properties |
| Melting point | 162-164 °C(lit.) | | Boiling point | 283.4±33.0 °C(Predicted) | | density | 1.10±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | pka | 8.61±0.58(Predicted) | | form | Crystalline Powder | | color | Beige | | Water Solubility | Slightly soluble in water. | | BRN | 2935796 | | InChIKey | NSJVYHOPHZMZPN-UHFFFAOYSA-N | | CAS DataBase Reference | 16419-60-6(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | RTECS | ED7777777 | | HazardClass | IRRITANT | | HS Code | 29163990 |
| 2-Tolylboronic acid Usage And Synthesis |
| Description | 2-Methylphenylboronic acid is an important organic boronic acid compound, which is widely used in Suzuki cross-coupling reaction and has important application value in the fields of organic synthesis and medicine and chemical industry. | | Physical properties | beige crystalline powder | | Uses | suzuki reaction | | Uses | 2-Methylbenzeneboronic acid is a reagent used for Pd-catalyzed arylation using Suzuki-Miyaura cross-coupling in water, Ruthenium catalyzed direct arylation reactions, Ligand-free copper-catalyzed coupling reactions, Rhodium-catalyzed asymmetric 1,4-addition reactions. Reagent used in Preparation of chiral monophosphorus ligands in asymmetric Suzuki-Miyaura coupling reaction, Human farnesyl pyrophosphate synthase inhibitors as antitumor agents for multiple myeloma cells |
| 2-Tolylboronic acid Preparation Products And Raw materials |
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