|  | |  |  | 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 acidsMannich-type multicomponent assembly and 1,3-dipolar cycloaddition for synthesis of tetrahydroisoquinoline fused isoxazolidine scaffordSuzuki-Miyaura cross-coupling of aryl and heteroaryl halidesOxidative Heck reaction for synthesis of functionalized cinnamaldehyde derivativesIntramolecular 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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