cis-ROSE OXIDE

Datasheet MSDS
Catalog Number
AFF1117
Product Name
cis-ROSE OXIDE
Structure
cis-ROSE OXIDE
CAS Number
3033-23-6
IUPAC Name
(2S,4R)-4-methyl-2-(2-methylprop-1-enyl)oxane
Synonyms
2H-Pyran,tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-,(2S-cis)-; l-tetrahydro-4-methyl-2-(2-methylpropenyl)-2H-Pyran; tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-,(2S-cis)-2H-Pyran; (2S-cis)-tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-2H-pyran; (-)-cis-roseoxide,tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-2,5-cis-2H-pyran,(-)-cis-roseoxide; 2H-Pyran,tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-,(2S,4R)-; Rosenoxidlinks; (-)-CIS-ROSEOXIDE
Molecular Formula
C10H18O
Molecular Weight
154.24
Appearance
colorless liquid
Purity
99.0%(sum of isomers)
Solubility
Insoluble in water; soluble in alcohol.
Boiling Point
194.97°C(EPI 4.0)
Storage
Store tightly sealed under inert gas in a cool, well-ventilated area.
Description
Intermediate in sugar metabolism and in enzymatic carbohydrate degradation (alcoholic fermentation) where it is converted to acetaldehyde and CO2 by carboxylase. In muscle, Pyruvic acid (derived from glycogen) is reduced to lactic acid during exertion, which is reoxidized and partially retransformed to glycogen during rest. The liver can convert Pyruvic acid to alanine by amination. A diagnostic agent for Parkinson disease.
SMILES
C[C@@H]1CCO[C@@H](C1)C=C(C)C
InChI
InChI=1S/C10H18O/c1-8(2)6-10-7-9(3)4-5-11-10/h6,9-10H,4-5,7H2,1-3H3/t9-,10-/m1/s1
InChI Key
CZCBTSFUTPZVKJ-NXEZZACHSA-N
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