264598
1,4-Benzodioxan-6-carboxaldehyde
98%
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About This Item
Productos recomendados
assay
98%
form
solid
bp
105 °C/15 mmHg (lit.)
mp
50-52 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)c1ccc2OCCOc2c1
InChI
1S/C9H8O3/c10-6-7-1-2-8-9(5-7)12-4-3-11-8/h1-2,5-6H,3-4H2
InChI key
CWKXDPPQCVWXAG-UHFFFAOYSA-N
Application
1,4-Benzodioxan-6-carboxaldehyde has been used:
- as building block in the synthesis of tetrahydroisoquinolinones
- in the preparation of benzofuran analog, a potential inhibitor of CAMP-specific phosphodiesterase type IV
- in the synthesis of (5Z)-5-(2,3-dihydro-1,4-benzodioxan-6-ylmethylene)-1-methyl-2-thioxoimidazolidin-4-one
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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Molecules (Basel, Switzerland), 16(9), 7377-7390 (2011-09-01)
A practical protocol for the preparation of (5Z)-2-alkylthio-5-arylmethylene-1-methyl-1,5-dihydro-4H-imidazol-4-one derivatives is reported. The new compounds were obtained in good yield and stereoselectivity in two steps, namely a solvent-free Knoevenagel condensation under microwave irradiation, followed by an S-alkylation reaction with various halogenoalkanes.
Structure-activity relationships involving the catechol subunit of rolipram.
Bioorganic & Medicinal Chemistry Letters, 4(15), 1855-1860 (1994)
Bioorganic & medicinal chemistry letters, 9(9), 1305-1310 (1999-05-26)
A new technique for high throughput solid phase synthesis using the centrifuge based liquid removal from readily available standard microtiterplates is described. This technique eliminates the filtration step and is therefore applicable to simultaneous processing of an unlimited number of
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