| Identification | More | [Name]
2-Ethoxycarbonylbenzeneboronic acid | [CAS]
380430-53-5 | [Synonyms]
2-CARBETHOXY-PHENYL-BORONIC ACID
2-ETHOXYCARBONYLBENZENEBORONIC ACID
2-ETHOXYCARBONYLPHENYLBORONIC ACID
ETHYL 2-BORONOBENZOATE
O-ETHOXYCARBONYLPHENYLBORONIC ACID
Ethyl 2-Boronobenzoat
2-ETHOXYCARNONYLPHENYLBORNIC ACID
Benzoic acid, 2-borono-, 1-ethyl ester (9CI)
2-(Ethoxycarbonyl)Phenylboroni | [Molecular Formula]
C9H11BO4 | [MDL Number]
MFCD02179453 | [Molecular Weight]
193.99 | [MOL File]
380430-53-5.mol |
| Chemical Properties | Back Directory | [Melting point ]
137 °C | [Boiling point ]
367.5±44.0 °C(Predicted) | [density ]
1.21±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
soluble in Methanol | [form ]
powder or crystals | [pka]
8.18±0.53(Predicted) | [color ]
White to Light yellow to Light orange | [InChI]
1S/C9H11BO4/c1-2-14-9(11)7-5-3-4-6-8(7)10(12)13/h3-6,12-13H,2H2,1H3 | [InChIKey]
QZKVVOXAEBCLPZ-UHFFFAOYSA-N | [SMILES]
CCOC(=O)c1ccccc1B(O)O | [CAS DataBase Reference]
380430-53-5(CAS DataBase Reference) |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3 | [HazardClass ]
IRRITANT | [HS Code ]
29319090 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Uses]
Reactant for:
- Synthesis of embelin derivatives via Suzuki-Miyaura reaction, cross metathesis and Wittig olefination
- Asymmetric cyclopropanation of alkenes with di-Me diazomalonate catalyzed by chiral diene-rhodium complexes
- Preparation of phenylalanines as selective AMPA- and kainate receptor ligands
- Preparation of aryl pyrazinones via microwave-assisted palladium-catalyzed arylation of resin supported pyrazinones under simultaneous cooling condition
- Regioselective preparation of (aryl)hydroxyquinolines via Suzuki-Miyaura cross-coupling with chloro(tosyloxy)quinoline under anhydrous conditions followed by nucleophilic deprotection of the tosyl group
| [Uses]
suzuki reaction |
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