Substance
ID:340824
Names and Identifiers
IUPAC Traditional name
2H-1,3-benzodioxol-5-ylboronic acid
IUPAC name
(2H-1,3-benzodioxol-5-yl)boronic acid
Synonyms
3,4-(亚甲基二氧基)苯硼酸1,3-Benzodioxole-5-boronic acid3,4-(Methylenedioxy)phenylboronic acid
Properties
Physical Property
Melting Point
224-229 °C(lit.)
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class
3
MSDS Link
Product Information
Empirical Formula (Hill Notation)
C7H7BO4
Molecule Details
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
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
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
Application
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
Molecular Spectra
No Data Available
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References
No Data Available
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