IUPAC Name: | (2-ethoxycarbonylphenyl)boronic acid |
Description: | 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. |
Molecular Weight: | 193.99 |
Molecular Formula: | C9H11O4B |
Canonical SMILES: | B(C1=CC=CC=C1C(=O)OCC)(O)O |
InChI: | InChI=1S/C9H11BO4/c1-2-14-9(11)7-5-3-4-6-8(7)10(12)13/h3-6,12-13H,2H2,1H3 |
InChI Key: | QZKVVOXAEBCLPZ-UHFFFAOYSA-N |
Boiling Point: | 367.5 °C at 760 mmHg |
Melting Point: | 128-136 °C |
Flash Point: | Not applicable |
Purity: | ≥ 95 % |
Density: | 1.21 g/cm3 |
MDL: | MFCD02179453 |
LogP: | -0.45690 |
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Related Functional Groups
Boronic Acids and Esters
2-(7,8-Difluoro-1-naphthyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-(3-((4-Bromo-2-chlorophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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