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| 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
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| 3,4-METHYLENEDIOXYPHENYLBORONIC ACID Preparation Products And Raw materials |
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