576638
trans-1-Propen-1-ylboronic acid
≥95.0%
Sinónimos:
(E)-1-Propen-1-ylboronic acid, (E)-Prop-1-enylboronic acid, trans-1-Propeneboronic acid, trans-1-Propenylboronic acid, trans-Propenylboronic acid
About This Item
Productos recomendados
Quality Level
assay
≥95.0%
impurities
~10 wt. % cis-isomer
mp
123-127 °C (lit.)
storage temp.
2-8°C
SMILES string
[H]\C(C)=C(\[H])B(O)O
InChI
1S/C3H7BO2/c1-2-3-4(5)6/h2-3,5-6H,1H3/b3-2+
InChI key
CBMCZKMIOZYAHS-NSCUHMNNSA-N
Application
- Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions
- Cu(II)-mediated Ullmann-type coupling
Reactant for preparation of:
- Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases
- Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling
- Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization
- Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones
- Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions[1][2][3]
- Cu(II)-mediated Ullmann-type coupling[4]
- Palladium-catalyzed Sonogashira cross-coupling[5]
Reactant for preparation of
- Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases[6]
- Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling[7]
- Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization[8]
- Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones[9]
Other Notes
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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