|
| | 3,4-METHYLENEDIOXYPHENYLBORONIC ACID Basic information |
| | 3,4-METHYLENEDIOXYPHENYLBORONIC ACID Chemical Properties |
| Melting point | 224-229 °C(lit.) | | Boiling point | 347.3±52.0 °C(Predicted) | | density | 1.42±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | pka | 8.48±0.20(Predicted) | | form | Powder | | color | White to off-white | | BRN | 5523347 | | InChIKey | CMHPUBKZZPSUIQ-UHFFFAOYSA-N | | CAS DataBase Reference | 94839-07-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 37/39-26 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29163990 |
| | 3,4-METHYLENEDIOXYPHENYLBORONIC ACID Usage And Synthesis |
| Chemical Properties | 3,4-METHYLENEDIOXYPHENYLBORONIC ACID is white powder
| | Uses | Reactant involved in:• ;Petasis reaction between glyoxylic acid, α-amino phosphonates, and organylboronic acids1• ;Mannich-type multicomponent assembly and 1,3-dipolar cycloaddition for synthesis of tetrahydroisoquinoline fused isoxazolidine scafford2• ;Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides3,4• ;Oxidative Heck reaction for synthesis of functionalized cinnamaldehyde derivatives5• ;Intramolecular Alder-ene and Pictet-Spengler reactions for synthesis of crinine6 | | Uses | suzuki reaction | | Uses | 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
|
| | 3,4-METHYLENEDIOXYPHENYLBORONIC ACID Preparation Products And Raw materials |
|