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About This Item
Empirical Formula (Hill Notation):
C6H10O3
CAS Number:
Molecular Weight:
130.14
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-963-3
Beilstein/REAXYS Number:
80957
MDL number:
Assay:
99%
Form:
solid
Quality Level
assay
99%
form
solid
optical activity
[α]25/D −49.8°, c = 2 in H2O
bp
120-122 °C/15 mmHg (lit.)
mp
91 °C (lit.)
functional group
ester, hydroxyl
SMILES string
CC1(C)COC(=O)[C@@H]1O
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3/t4-/m0/s1
InChI key
SERHXTVXHNVDKA-BYPYZUCNSA-N
Application
D-(-)-Pantolactone is a chiral auxiliary used in many asymmetric synthesis reactions.
It can be used as a chiral starting material to synthesize:
It can be used as a chiral starting material to synthesize:
- An insect sex pheromone named 1S,2S,3R-1-acetoxymethyl-2,3,4,4-tetrameth-ylcyclopentane.
- (-)-Enantiomer of (R)-8-hydroxy-4,7,7-trimethyl-7,8-dihydrocyclopenta[e]isoindole-1,3(2H,6H)-dione, a norsesquiterpene alkaloid.
- A bicyclic diterpene named isofregenedadiol.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Find documentation for the products that you have recently purchased in the Document Library.
Total synthesis of an anticancer norsesquiterpene alkaloid isolated from the fungus Flammulina velutipes
Kashinath K, et al.
Organic & Biomolecular Chemistry, 12(24), 4098-4103 (2014)
Total synthesis of isofregenedadiol
Kurhade SE, et al.
Organic Letters, 13(14), 3690-3693 (2011)
Asymmetric diels alder reactions and michael type additions with 6 (R)-3′(R)-Pantolactone-substituted-2H-pyran-3 (6H)-one.
Knol J, et al.
Tetrahedron Letters, 32(50), 7465-7468 (1991)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 237817-25G | 04061838786265 |
| 237817-5G | 04061838786272 |
