furan-2-acetic acid

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Company Name: Beijing HwrkChemical Technology Co., Ltd  
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furan-2-acetic acid manufacturers

  • furan-2-acetic acid
  • furan-2-acetic acid pictures
  • $6.60
  • 2020-01-03
  • CAS:2745-26-8
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 1kg -1000kg
furan-2-acetic acid Basic information
Product Name:furan-2-acetic acid
Synonyms:furan-2-acetic acid;2-FURYLACETIC ACID;(Furan-2-yl)acetic acid;2-(2-furyl)acetic acid;2-furan-2-ylacetic acid;2-furan-2-ylethanoic acid;2-Furanylacetic acid;2-Furanacetic acid 97%
CAS:2745-26-8
MF:C6H6O3
MW:126.11
EINECS:220-380-3
Product Categories:Building Blocks;C4 to C7;Chemical Synthesis;Furans;Heterocyclic Building Blocks
Mol File:2745-26-8.mol
furan-2-acetic acid Structure
furan-2-acetic acid Chemical Properties
Melting point 64-69 °C
Boiling point 234℃
density 1.265
refractive index 1.5627 (estimate)
Fp 95℃
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka4.16±0.10(Predicted)
color Dark Beige to Very Dark Yellow
InChI1S/C6H6O3/c7-6(8)4-5-2-1-3-9-5/h1-3H,4H2,(H,7,8)
InChIKeyVYSRZETUSAOIMP-UHFFFAOYSA-N
SMILESOC(=O)Cc1ccco1
Safety Information
Hazard Codes Xn
Risk Statements 22-37/38-41
Safety Statements 26-39
WGK Germany 3
HS Code 2932190090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
furan-2-acetic acid Usage And Synthesis
Uses2-(Furan-2-yl)acetic Acid is one of the compounds detected in tobacco smoke condensate.
DefinitionChEBI: 2-furanacetic acid is a heteroarene.
Synthesis
2-FURYLACETONITRILE

2745-25-7

furan-2-acetic acid

2745-26-8

The general procedure for the synthesis of 2-furanacetic acid from 2-(furan-2-yl)acetonitrile was as follows: to a solvent mixture of 30 mL of 3N sodium hydroxide solution and 30 mL of methanol, 3.34 g (31.2 mmol) of 2-(furan-2-yl)acetonitrile was added, and stirred until it was completely dissolved. The reaction mixture was heated to reflux for 2 hours and 30 minutes with continuous stirring. After completion of the reaction, the solution was cooled to room temperature and separated by extraction with ether. The aqueous phase was acidified with 20 mL of concentrated hydrochloric acid to release the organic products and extracted again with ether. The ether extracts were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 3.84 g (30.5 mmol) of 2-furanacetic acid in 97.8% yield.

References[1] Patent: US6215016, 2001, B1
[2] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1993, # 10, p. 1941 - 1946
[3] Collection of Czechoslovak Chemical Communications, 1980, vol. 45, # 5, p. 1361 - 1365
[4] Chemische Berichte, 1930, vol. 63, p. 749,753
[5] Journal of the American Chemical Society, 1930, vol. 52, p. 1284
furan-2-acetic acid Preparation Products And Raw materials
Raw materials2-FURYLACETONITRILE-->Carbon-->Methanol-->Hydrochloric acid-->Sodium hydroxide
Preparation Products(2-FURYL)GLYOXYLIC ACID-->furan-2-acetyl chloride
Tag:furan-2-acetic acid(2745-26-8) Related Product Information
Methyl benzofuran-2-acetate (2-FURYL)GLYOXYLIC ACID furan-2-acetic acid 2-Methylfuran-3-thiol acetate 2-Methoxyiminofurylacetic acid amonium salt (Z)-2-Methoxyimino-2-(furyl-2-yl) acetic acid ammonium salt 2,3-Dihydro-alpha-hydroxy-5-benzofuranacetic acid (R)-BENZYLOXYCARBONYLAMINO-FURAN-2-YL-ACETIC ACID alpha-(methoxyimino)furan-2-acetic acid (S)-AMINO-FURAN-2-YL-ACETIC ACID AMINO-FURAN-2-YL-ACETIC ACID CBZ-2-AMINO-2-FURANACETIC ACID 2-(2-FURYL)SUCCINIC ACID (Z)-alpha-(methoxyimino)furan-2-acetic acid 2-Benzofuranacetic acid (5-Butyl-3-oxo-2,3-dihydrofuran-2-yl)-acetic acid syn-2-Methoxy-imino-2-(2-furyl)-acetic acid, ammomium salt, 99+% (Furylacryloyloxy)triethyl plumbane