310336
cis-4,7-Dihydro-1,3-dioxepin
97%
Synonym(s):
cis-1,3-Dioxep-5-ene
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About This Item
Empirical Formula (Hill Notation):
C5H8O2
CAS Number:
Molecular Weight:
100.12
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
liquid
refractive index
n20/D 1.457 (lit.)
bp
125-127 °C (lit.)
density
1.049 g/mL at 25 °C (lit.)
functional group
ether
SMILES string
C1OCC=CCO1
InChI
1S/C5H8O2/c1-2-4-7-5-6-3-1/h1-2H,3-5H2
InChI key
BAKUAUDFCNFLBX-UHFFFAOYSA-N
General description
4,7-dihydro-1,3-dioxepin derivatives undergoes hydroformylation to form optically active aldehydes[1].
Signal Word
Warning
Hazard Statements
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
78.8 °F - closed cup
Flash Point(C)
26 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Toshihide Horiuchi et al.
The Journal of organic chemistry, 62(13), 4285-4292 (1997-06-27)
Asymmetric hydroformylation of heterocyclic olefins catalyzed by phosphine-phosphite-Rh(I) complexes has been investigated. Hydroformylation of symmetrical heterocyclic olefins such as 2,5-dihydrofuran, 3-pyrroline derivatives, and 4,7-dihydro-1,3-dioxepin derivatives afforded the optically active aldehydes as single products in 64-76% ee. Unsymmetrical substrates such as
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