5-CHLORO-2-FURALDEHYDE
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
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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ALFA
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.
References
[1] Chemistry - A European Journal, 2016, vol. 22, # 1, p. 129 - 133
[2] Patent: WO2004/33440, 2004, A1. Location in patent: Page 238
[3] Patent: US2004/147559, 2004, A1. Location in patent: Page 121
[4] Patent: US2004/106794, 2004, A1. Location in patent: Page 122
[5] Patent: WO2005/66147, 2005, A1. Location in patent: Page/Page column 207
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