Search
Element Search
Structure Search
Thermo Scientific Chemicals
1,3-Cyclopentanedione, 98%
CAS: 3859-41-4 | C5H6O2 | 98.10 g/mol
Have Questions?
Change view
Catalog number L10336.06
also known as L10336-06
Price (USD)
153.65
Online Exclusive
171.00Save 17.35 (10%)
Each
Quantity:
5 g
Price (USD)
153.65
Online Exclusive
171.00Save 17.35 (10%)
Each
Chemical Identifiers
CAS3859-41-4
IUPAC Namecyclopentane-1,3-dione
Molecular FormulaC5H6O2
InChI KeyLOGSONSNCYTHPS-UHFFFAOYSA-N
SMILESO=C1CCC(=O)C1
View more
Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Appearance (Color)Cream to yellow to brown
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Assay (HPLC)≥97.5%
1,3 cyclopentanedione is used in the synthesis of pgd2 . Reatant in the synthesis of fused dihydrofuran.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,3 cyclopentanedione is used in the synthesis of pgd2 . Reatant in the synthesis of fused dihydrofuran.
Solubility
Very soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
1,3 cyclopentanedione is used in the synthesis of pgd2 . Reatant in the synthesis of fused dihydrofuran.
Solubility
Very soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
General References:
- Gianfranco Cainelli,; Daria Giacomini,; Mauro Panunzioa,; Giorgio Martelli,; Giuseppe Spunta. Prostagland1ns:total synthesis of pgd2 via 1,3 cyclopentanedione. Tetrahedron. 1985, 41 (7), 1385-1392.
- Jiang Qian,; Chananat Klomsiri,; Marcus W. Wright,; S. Bruce King. Simple synthesis of 1,3-cyclopentanedione derived probes for labelingsulfenic acid proteins. Chem. Commun., 2011 , 47 9203-9205.
- Reaction with 1,3,5-trioxane yields a fused 1,3-dioxin intermediate, useful as a ß -keto vinyl cation equivalent: Org. Synth., 75, 189 (1997):