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5-CHLORO-2-FURALDEHYDE

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5-CHLORO-2-FURALDEHYDE Basic information

Product Name:
5-CHLORO-2-FURALDEHYDE
Synonyms:
  • TIMTEC-BB SBB004223
  • 5-CHLORO-2-FURALDEHYDE,97%
  • 5-CHLORO-2-FURALDEHYDE, 98+%
  • 5-Chloro-2-furaldehyde, 98%, stab. with 2% ethanol
  • 5-Chloro-2-furaldehyde,97%,stabilized
  • 5-Chloro-2-furaldehyde, stabilized, 97%
  • 5-CHLORO-2-FURALDEHYDE
  • 5-chlorofuran-2-carboxaldehyde
CAS:
21508-19-0
MF:
C5H3ClO2
MW:
130.53
EINECS:
627-276-0
Product Categories:
  • Building Blocks
  • Furans
  • FuransHeterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Aldehydes
  • Building Blocks
  • C1 to C6
  • C4 to C7
  • C4 to C8
  • Carbonyl Compounds
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Organic Building Blocks
Mol File:
21508-19-0.mol
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5-CHLORO-2-FURALDEHYDE Chemical Properties

Melting point:
34-37 °C (lit.)
Boiling point:
70°C 10mm
Density 
1.361±0.06 g/cm3(Predicted)
Flash point:
190 °F
storage temp. 
2-8°C
solubility 
Acetone (Slightly), Methanol (Slightly)
form 
Crystalline Powder
color 
White to off-white
Water Solubility 
Insoluble in water.
Sensitive 
Air Sensitive
BRN 
108401
Exposure limits
ACGIH: STEL 1000 ppm
OSHA: TWA 1000 ppm(1900 mg/m3)
NIOSH: IDLH 3300 ppm; TWA 1000 ppm(1900 mg/m3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29321900

MSDS

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5-CHLORO-2-FURALDEHYDE Usage And Synthesis

Chemical Properties

White to yellow powder

Uses

(+)-1-Deoxynojirimycin hydrochloride interferes with normal processing of N-linked glycoproteins, producing reduced amounts of complex type oligosaccharides.

Uses

5-Chloro-2-furaldehyde may be used as an internal standard during the analysis of furanic compounds by reversed-phase-high performance liquid chromatography–diode array detection (RP-HPLC–DAD) method.

General Description

5-Chloro-2-furaldehyde is also known as 5-chlorofurfural. It reacts with aniline and aniline hydrochloride to form bis-(phenylamino) derivatives, without the furan ring cleavage. It also undergoes coupling with ethyl acetoacetate to form the corresponding ethyl bis-acetoacetate.

5-CHLORO-2-FURALDEHYDESupplier

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