2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID manufacturers
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| | 2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID Basic information |
| | 2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID Chemical Properties |
| Melting point | 231-233 | | Boiling point | 434.3±55.0 °C(Predicted) | | density | 1.49±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | form | powder | | pka | 8.13±0.20(Predicted) | | Appearance | Off-white to pale purple Solid | | InChI | 1S/C8H7BO5/c10-3-5-1-7-8(14-4-13-7)2-6(5)9(11)12/h1-3,11-12H,4H2 | | InChIKey | AKEPUIJBVDGLMX-UHFFFAOYSA-N | | SMILES | OB(O)c1cc2OCOc2cc1C=O |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 2 | | Hazard Note | Irritant | | HS Code | 2932990090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| | 2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID Usage And Synthesis |
| Uses | Reactant for:• ;Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes1• ;Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation2• ;Synthesis of oxazoline-substituted potassium organotrifluoroborates3• ;Preparation of aristolactam analogs as an antitumor agent4• ;Suzuki-Miyaura coupling reactions5• ;Suzuki and Negishi cross-coupling reactions6 | | Uses | Reactant for:
- Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes
- Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation
- Synthesis of oxazoline-substituted potassium organotrifluoroborates
- Preparation of aristolactam analogs as an antitumor agent
- Suzuki-Miyaura coupling reactions
- Suzuki and Negishi cross-coupling reactions
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| | 2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID Preparation Products And Raw materials |
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