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ChemicalBook--->CAS DataBase List--->94838-88-7

94838-88-7

94838-88-7 Structure

94838-88-7 Structure
IdentificationBack Directory
[Name]

2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID
[CAS]

94838-88-7
[Synonyms]

(6-formyl-1,3-benzodioxol-5-yl)boronic acid
6-FORMYLBENZO[D][1,3]DIOXOL-5-YLBORONIC ACID
2-FORMYL-4,5-METHYLENEDIOXYPHENYLBORONIC ACID
(6-formyl-2H-1,3-benzodioxol-5-yl)boronic acid
Boronic acid, B-(6-formyl-1,3-benzodioxol-5-yl)-
(2-FORMYL-4,5-METHYLENEDIOXY)BENZENEBORONIC ACID
2-Formyl-4,5-(methylenedioxy)benzeneboronic acid 95%
[Molecular Formula]

C8H7BO5
[MDL Number]

MFCD01319005
[MOL File]

94838-88-7.mol
[Molecular Weight]

193.95
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

2
[Hazard Note ]

Irritant
[HS Code ]

2932990090
Hazard InformationBack Directory
[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
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