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2(5H)-Furanone CAS NO.497-23-4

Min.Order Quantity:
1 Kilogram
Purity:
98%
Port:
China Main Port
Payment Terms:
L/C,D/A,D/P,T/T,MoneyGram,Other

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Product Details

Keywords

  • 2(5H)-Furanone
  • 497-23-4
  • C4H4O2

Quick Details

  • ProName: 2(5H)-Furanone
  • CasNo: 497-23-4
  • Molecular Formula: C4H4O2
  • Appearance: powder
  • Application: 497-23-4
  • DeliveryTime: within 3-7 days
  • PackAge: as requested
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Month
  • Purity: 98%
  • Storage: store in cool, dry place
  • Transportation: by sea or by air
  • LimitNum: 1 Kilogram

Superiority

2(5h)-furanone basic information
product name: 2(5h)-furanone
synonyms: .alpha.,.beta.-crotonolactone;.delta.,.alpha.,.beta.-butenolide;.gamma.-crotolactone;.gamma.-hydroxycrotonicacidlactone;2(5h)-furanone (.gamma.-crotonolactone);2-buten-4-olide;2-butenoic acid, 4-hydroxy-, gamma-lactone;2-butenoic acid-gamma-lactone
cas: 497-23-4
mf: c4h4o2
mw: 84.07
einecs: 207-839-3
product categories: heterocycles;building blocks;c4 to c7;chemical synthesis;furans;heterocyclic building blocks;antibiotic
mol file: 497-23-4.mol
2(5h)-furanone structure
2(5h)-furanone chemical properties
melting point 4-5 °c(lit.)
boiling point 86-87 °c12 mm hg(lit.)
density 1.185 g/ml at 25 °c(lit.)
refractive index n20/d 1.469(lit.)
fp 214 °f
storage temp. 2-8°c
brn 383585
cas database reference 497-23-4(cas database reference)
nist chemistry reference 2(5h)-furanone(497-23-4)
epa substance registry system 2(5h)-furanone(497-23-4)
safety information
hazard codes xi
risk statements 36/37/38
safety statements 26
wgk germany 3
rtecs lu3453000
f 8-10
hazard note irritant
hs code 29322980
msds information
provider language
furan-2(5h)-one english
sigmaaldrich english
alfa english
2(5h)-furanone usage and synthesis
chemical properties light brown liquid
usage 2-furanone is a heterocyclic organic compound that is used widely in the synthetic preparation of pharmaceutical goods.
usage a versatile reagent used in michael addition reactions1 for synthesis of lignans.2 also employed in three-component michael-aldol reactions with an aldehyde anda thiolate3 or carbanion.4
2(5h)-furanone preparation products and raw materials

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