ChemicalBook > CAS DataBase List > SPIRO[4.5]DECANE-7,9-DIONE

SPIRO[4.5]DECANE-7,9-DIONE

Product Name
SPIRO[4.5]DECANE-7,9-DIONE
CAS No.
82683-51-0
Chemical Name
SPIRO[4.5]DECANE-7,9-DIONE
Synonyms
SPIRO[4.5]DECANE-7,9-DIONE
CBNumber
CB4374882
Molecular Formula
C10H14O2
Formula Weight
166.22
MOL File
82683-51-0.mol
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SPIRO[4.5]DECANE-7,9-DIONE Property

Melting point:
136 °C
Boiling point:
314.0±25.0 °C(Predicted)
Density 
1.10±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
9.40±0.20(Predicted)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
4505AJ
Product name
Spiro[4.5]decane-7,9-dione
Packaging
100mg
Price
$124
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0165935
Product name
SPIRO[4.5]DECANE-7,9-DIONE
Purity
98.00%
Packaging
5MG
Price
$495.45
Updated
2021/12/16
Arctom
Product number
AS481320
Product name
Spiro[4.5]decane-7,9-dione
Purity
97%
Packaging
100mg
Price
$50
Updated
2021/12/16
Arctom
Product number
AS481320
Product name
Spiro[4.5]decane-7,9-dione
Purity
97%
Packaging
250mg
Price
$79
Updated
2021/12/16
Arctom
Product number
AS481320
Product name
Spiro[4.5]decane-7,9-dione
Purity
97%
Packaging
1g
Price
$192
Updated
2021/12/16
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SPIRO[4.5]DECANE-7,9-DIONE Chemical Properties,Usage,Production

Uses

Spiro[4.5]decane-7,9-dione (Compound 2e) is a cyclic 1,3-diketone. Spiro[4.5]decane-7,9-dione can be used in the study of glioma tumors[1].

Synthesis

933-02-8

105-53-3

82683-51-0

GENERAL STEPS: A mixture of 1-cyclopentadienylpropan-2-one (1 g, 9.4 mmol) and diethyl malonate (1.75 g, 11 mmol) was slowly added dropwise to a sodium methanolate solution prepared from sodium metal (0.25 g, 11 mmol) dissolved in methanol (3 mL). The reaction mixture was heated under reflux conditions for 2 hours. Subsequently, a hot solution of barium hydroxide (11.23 g, 73 mmol) dissolved in 100 mL of water was added to the reaction system and reflux was continued for 24 hours. After the reaction was completed, it was neutralized to pH 6 with dilute hydrochloric acid and filtered while hot. The filtrate was cooled, acidified to pH 1 with dilute hydrochloric acid, refluxed again for 15 min, filtered while hot and cooled. The precipitated solid was filtered, washed with water and dried to give 0.87 g (56% yield) of spiro[4.5]decane-7,9-dione.

References

[1] Alexander R, et al. 4-(1,3-Thiazol-2-yl)morpholine derivatives as inhibitors of phosphoinositide 3-kinase. Bioorg Med Chem Lett. 2008 Aug 1;18(15):4316-20. DOI:10.1016/j.bmcl.2008.06.076

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