2-Acetylfuran
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    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H558432

CAS#: 1192-62-7

Description: 2-Acetylfuran is a uricosuric drug. It is used to effectively to control hyperuricemia in renal transplantation


Chemical Structure

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2-Acetylfuran
CAS# 1192-62-7

Theoretical Analysis

Hodoodo Cat#: H558432
Name: 2-Acetylfuran
CAS#: 1192-62-7
Chemical Formula: C6H6O2
Exact Mass: 110.04
Molecular Weight: 110.110
Elemental Analysis: C, 65.45; H, 5.49; O, 29.06

Price and Availability

Size Price Availability Quantity
25g USD 200 2 Weeks
500g USD 580 2 Weeks
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Synonym: 2-Acetylfuran; 2 Acetylfuran; 2Acetylfuran; Acetylfuran; NSC 4665; NSC 49133;

IUPAC/Chemical Name: 2-Furyl methyl ketone

InChi Key: IEMMBWWQXVXBEU-UHFFFAOYSA-N

InChi Code: InChI=1S/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H3

SMILES Code: O=C(C1=CC=CO1)C

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.03.00

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 110.11 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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6: Corsi G, Valentini F. [Acute hepatitis in subjects exposed to 2-acetylfuran and hydrazine]. Med Lav. 1983 Jul-Aug;74(4):284-90. Italian. PubMed PMID: 6664322.

7: Liu Y, Rowley CN, Kerton FM. Combined experimental and computational studies on the physical and chemical properties of the renewable amide, 3-acetamido-5-acetylfuran. Chemphyschem. 2014 Dec 15;15(18):4087-94. doi: 10.1002/cphc.201402376. Epub 2014 Oct 24. PubMed PMID: 25346518.

8: Wang Y, Ho CT. Comparison of 2-acetylfuran formation between ribose and glucose in the Maillard reaction. J Agric Food Chem. 2008 Dec 24;56(24):11997-2001. doi: 10.1021/jf802683a. PubMed PMID: 19090713.

9: Magauer T, Myers AG. Short and efficient synthetic route to methyl α-trioxacarcinoside B and anomerically activated derivatives. Org Lett. 2011 Oct 21;13(20):5584-7. doi: 10.1021/ol202315m. Epub 2011 Sep 29. PubMed PMID: 21958151; PubMed Central PMCID: PMC3216050.

10: Kawai T, Yasugi T, Mizunuma K, Horiguchi S, Uchida Y, Iwami O, Iguchi H, Ikeda M. Dose-dependent increase in 2,5-hexanedione in the urine of workers exposed to n-hexane. Int Arch Occup Environ Health. 1991;63(4):285-91. PubMed PMID: 1743771.

11: Chandra S, Kumar A. Spectral studies on Co(II), Ni(II) and Cu(II) complexes with thiosemicarbazone (L1) and semicarbazone (L2) derived from 2-acetyl furan. Spectrochim Acta A Mol Biomol Spectrosc. 2007 Apr;66(4-5):1347-51. Epub 2006 Jul 11. PubMed PMID: 16919999.

12: Seebaluck R, Gurib-Fakim A, Mahomoodally F. Medicinal plants from the genus Acalypha (Euphorbiaceae)--a review of their ethnopharmacology and phytochemistry. J Ethnopharmacol. 2015 Jan 15;159:137-57. doi: 10.1016/j.jep.2014.10.040. Epub 2014 Oct 30. Review. PubMed PMID: 25446604.

13: Condurso C, Cincotta F, Verzera A. Determination of furan and furan derivatives in baby food. Food Chem. 2018 Jun 1;250:155-161. doi: 10.1016/j.foodchem.2017.12.091. Epub 2018 Jan 2. PubMed PMID: 29412906.