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Home > Encyclopedia > 5-CHLORO-2-FURALDEHYDE

5-CHLORO-2-FURALDEHYDE

5-CHLORO-2-FURALDEHYDE structure

5-CHLORO-2-FURALDEHYDE 

structure
  • CAS No:

    21508-19-0

  • Formula:

    C5H3ClO2

  • Chemical Name:

    5-CHLORO-2-FURALDEHYDE

  • Synonyms:

    TIMTEC-BB SBB004223;5-CHLORO-2-FURALDEHYDE;5-chlorofuran-2-carboxaldehyde;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%

  • Categories:

    Organic Chemistry  >  Aldehydes

Description

White to yellow powder

5-CHLORO-2-FURALDEHYDE Basic Attributes

130.53

129.982162

108401

-0

2932190090

Characteristics

30.2

1.7

White to off-white Crystalline Powder

1.4±0.1 g/cm3

34-37 °C(lit.)

70°C10mm

190 °F

1.543

Insoluble in water.

2-8°C

0.553mmHg at 25°C

Safety Information

NONH for all modes of transport

3

36/37/38

26-36

Xi

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 43 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

5-CHLORO-2-FURALDEHYDE Use and Manufacturing

The aldehyde (3.5g) and conc. HCI (20MUT) were combined and stirred overnight at 40°C. The reaction mixture was poured into cold water and extracted with ether, washed with satd. NAHCO3 AND brine, dried over anhydrous MGS04, filtered and concentrated in vacuo to give 1.76g of product (55percent)The aldehyde (3.5 g) and cone. HC1 (20 ml) were combined and stirred overnight at 40 C. The reaction mixture was poured into cold water and extracted with ether, washed with satd. NaHCO3 and brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to give 1.76 g of product (55percent)The aldehyde (3.5 g) and conc. HCl (20 ml) were combined and stirred overnight at 40 C. The reaction mixture was poured into cold water and extracted with ether, washed with satd. NaHCO3 and brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to give 1.76 g of product (55percent)PREPARATIVE EXAMPLE 34.1; The aldehyde (3.5g) and conc. HCI (20ml) were combined and stirred overnight at 40°C. The reaction mixture was poured into cold water and extracted with ether, washed with satd. NaHCO3 and brine, dried over anhydrous MgS04, filtered and concentrated in vacuo to give 1.76g of product (55percent)The aldehyde (3.5g) and conc. HCl(20ml) were combined and stirred overnight at 40°C. The reaction mixture was poured into cold water and extracted with ether, washed with satd. NaHCO3 and brine, dried over anhydrous MgS04, filtered and concentrated in vacuo to give 1.76g of product (55percent)

Computed Properties

Molecular Weight:130.53
XLogP3:1.7
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:129.9821570
Monoisotopic Mass:129.9821570
Topological Polar Surface Area:30.2
Heavy Atom Count:8
Complexity:94.4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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