1,3-CYCLOPENTANEDIONE |
PRODUCT
IDENTIFICATION
|
CAS
NO. |
3859-41-4 |
|
EINECS NO. |
223-372-8 |
FORMULA |
C5H6(=O)2 |
MOL
WT. |
98.10 |
H.S.
CODE |
|
TOXICITY
|
|
SYNONYMS |
Cyclopentane-1,3-dione;
1,3-Cyclopentadione; |
3-Hydroxy-2-cyclopenten-1-one;
|
SMILES
|
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CLASSIFICATION
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DIKETONES
/
|
PHYSICAL AND CHEMICAL PROPERTIES
|
PHYSICAL
STATE |
white to off-white
crystalline powder |
MELTING POINT |
147
- 151 C |
BOILING
POINT |
|
SPECIFIC GRAVITY |
|
SOLUBILITY
IN WATER |
|
pH |
|
VAPOR DENSITY |
|
AUTOIGNITION
|
|
NFPA
RATINGS
|
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REFRACTIVE
INDEX
|
|
FLASH
POINT |
|
STABILITY |
Stable
under ordinary conditions
|
APPLICATIONS
|
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.
|
SALES
SPECIFICATION |
APPEARANCE
|
white to off-white
crystalline powder |
PURITY |
98.0%
min |
MELTING POINT |
147
- 151 C |
TRANSPORTATION |
PACKING |
|
HAZARD CLASS |
|
UN
NO. |
|
OTHER
INFORMATION |
Hazard
Symbols: , Risk Phrases: , Safety Phrases: 22-24/25 |
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