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g-Crotonolactone

gamma-crotonolactone

CAS: 497-23-4

Molecular Formula: C4H4O2

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g-Crotonolactone - Names and Identifiers

Name gamma-crotonolactone
Synonyms 5H-Furan-2-one
2(5H)-Furanone
furan-2(5H)-one
2-(5H)-furanone
g-Crotonolactone
a,b-Crotonolactone
2,5-Dihydrofuranone
gamma-crotonolactone
2,5-Dihydrofuran-2-one
Crotonic acid, 4-hydroxy-
.alpha.,.beta.-Crotonolactone
5-Oxo-2,5-dihydrofuran-3-yl ester
γ-Crotonolactone, 2-Buten-1,4-olide
2-Buten-1,4-olide~gamma-Crotonolactone
2(5H)-Furanone,γ-Crotonolactone, 2-Buten-1,4-olide
CAS 497-23-4
EINECS 207-839-3
InChI InChI=1/C4H4O2/c5-4-2-1-3-6-4/h1-2H,3H2
InChIKey VIHAEDVKXSOUAT-UHFFFAOYSA-N

g-Crotonolactone - Physico-chemical Properties

Molecular FormulaC4H4O2
Molar Mass84.07
Density1.185 g/mL at 25 °C (lit.)
Melting Point4-5 °C (lit.)
Boling Point86-87 °C/12 mmHg (lit.)
Flash Point214°F
JECFA Number2000
Water SolubilityImmiscible with water.
Solubility Chloroform, Ethyl Acetate (Slightly)
Vapor Presure0.273mmHg at 25°C
AppearanceLiquid
ColorClear colorless to pale yellow or amber
BRN383585
Storage Condition2-8°C
StabilityMoisture Sensitive
Refractive Indexn20/D 1.469(lit.)
Physical and Chemical Properties
density:
1.185

g-Crotonolactone - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany3
RTECSLU3453000
FLUKA BRAND F CODES8-10
HS Code29322980
Hazard NoteIrritant

g-Crotonolactone - Reference Information

FEMA4138 | 4-HYDROXY-2-BUTENOIC ACID GAMMA-LACTONE
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
Introduction 2(5h)-furanone, also known as γ-crotonolactone, 5h-furan-2-one, etc., is an organic heterocyclic compound, is the simplest crotonolactone, colorless liquid at room temperature, its structural formula is γ-crotonyl lactone, which is a precursor material of many active molecules of drugs, and its structure is commonly found in bioactive molecules, such as antibiotics, antibiotics, anti-tumor and antiviral drugs.
preparation at room temperature, add 1(26g,0.2 mol) to acetone (1000 mL) A molar concentration of 0.2 mol is formed in the solution. H2O(10
mL) was added to the L-1 organic solution, and hydrochloric acid (1 mL) was added dropwise under vigorous stirring. After addition, stirring was continued for 12 hours at room temperature, carefully add solid sodium bicarbonate and neutral, diatomite filtration, dichloromethane washing, combined
filtrate, vacuum distillation to remove most of the organic solvent, add water, aqueous layer is extracted with dichloromethane, combined organic layer, anhydrous magnesium sulfate
dried, filtered, the filtrate was distilled at atmospheric pressure to remove the solvent, and the remaining liquid column chromatography (dichloromethane/methanol) gave 2(5h)-furanone 7(14g,82%).
biological activity 2(5h)-Furanone is an endogenous metabolite.
toxic substance data information provided by: pubchem.ncbi.nlm.nih.gov (external link)
Last Update:2024-04-09 21:04:16
g-Crotonolactone
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View History
g-Crotonolactone
高铼酸
876-17-5
1-OCTYLSODIUMSULFONATE
TURIN
ETHYL SODIUM OXALACETATE
111-06-8
3125-64-2
PHENOL REAGENT NO 2
55-16-3
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