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2-ETHYL-1,3-CYCLOPENTANEDIONE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 823-36-9 | |
EINECS NO. | 212-512-3 | |
FORMULA | C7H10O2 | |
MOL WT. | 126.15 | |
H.S. CODE |
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TOXICITY |
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SYNONYMS | 2-Ethylcyclopentane-1,3-dione; 2-Ethyl-1,3-cyclopentadione; | |
2-Etilciclopentano-1,3-diona; 2-éthylcyclopentane-1,3-dione; | ||
SMILES |
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CLASSIFICATION |
DIKETONES / |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white to yellow crystalline powder | |
MELTING POINT |
173 - 176 C | |
BOILING POINT | ||
SPECIFIC GRAVITY | ||
SOLUBILITY IN WATER |
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pH |
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VISCOSITY | ||
AUTOIGNITION |
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REFRACTIVE INDEX |
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NFPA RATINGS | ||
FLASH POINT |
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STABILITY | Stable under normal conditions. Moisture sensitive. | |
GENERAL DESCRIPTION & APPLICATIONS |
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1,3-Cyclopentanedione
is a
cyclic 1,3-diketone which two ketones are separated only by one
carbon. The beta-ketone is stable as a conjugated enol rather than
alpha-diketone due to the delocalization which makes the counter ion more stable
and less likely to regain the proton. 1,3-Diketone and its esters contain active methylene groups which have relatively acidic
alpha-protons due to H atom adjacent to two carbonyl groups. The reactivity of
its methylene group provide the sequence of reactions of alkylation, hydrolysis
of the esters and decarboxylation resulting in substituted ketones. The
methylene group can be reacted to form amino-carbonyl
compounds. 1,3-Diketone compounds (beta-ketones) include malonic
acid, diethyl malonate, Meldrum's acid, and acetoacetic acid derivatives.
1,3-Cyclopentanedione is a versatile reagent for synthesis of perhydroazulenes, prostaglandin products (biologically active unsaturated 20-carbon fatty acids including a 5-carbon ring, derived enzymatically ), and Knoevenagel products. |
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SALES SPECIFICATION | ||
APPEARANCE |
yellow crystalline powder | |
CONTENT |
98.0% min |
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REFRACTIVE INDEX |
173 - 176 C | |
TRANSPORTATION | ||
PACKING | ||
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: XI, Risk Phrases: 36/37/38, Safety Phrases: 22-24/25 |
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