488-93-7

3-Furanoic acid Chemical Structure
488-93-7

Chemical Structure

3-Furanoic acid

  • CAS No.: 488-93-7
  • Formula:C5H4O3
  • Molecular Weight:112.08

IUPAC Name: furan-3-carboxylic acid

InChIKey: IHCCAYCGZOLTEU-UHFFFAOYSA-N

SMILES: O=C(O)C1=COC=C1

Biological Activity: 3-Furanoic acid is an active unit, and its derivatives have a wide range of anti-inflammatory activities. 3-Furanoic acid-related derivatives can target inflammation-related signaling pathways and inhibit the proliferation of synovial fibroblasts to exert immunomodulatory effects[1][2][3].

Cat. No. Nom du produit Pureté Description Pricing
HY-21075
3-Furanoic acid 99.97% 3-Furanoic acid is an active unit, and its derivatives have a wide range of anti-inflammatory activities. 3-Furanoic acid-related derivatives can target inflammation-related signaling pathways and inhibit the proliferation of synovial fibroblasts to exert immunomodulatory effects.
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HY-21075R
3-Furanoic acid (Standard) ≥98% 3-Furanoic acid (Standard) is the analytical standard of 3-Furanoic acid. This product is intended for research and analytical applications. 3-Furanoic acid is an active unit, and its derivatives have a wide range of anti-inflammatory activities. 3-Furanoic acid-related derivatives can target inflammation-related signaling pathways and inhibit the proliferation of synovial fibroblasts to exert immunomodulatory effects.
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HY-32004
Coumalic acid 97.65% Coumalic acid is an inhibitor of human carbonic anhydrase (hCA) (KI = 0.073 μM for hCA IX; KI = 0.083 μM for hCA XII). Coumalic acid is a valuable platform compound which can be prepared from malic acid. Coumalic acid can be used in the flavorings, fragrances and cosmetics industries, as polymer components, and pharmaceutical scaffolds. Coumalic acid displays antibronchial and antimalarial activity.
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HY-76224
3-Furaldehyde 99.98% 3-Furaldehyde is a member of furans and an aldehyde, and can be used to synthesize the neoclerodane diterpene Salvinorin A.
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HY-I0736
Isonicotinic acid 99.96% Isonicotinic acid is a pyridine carboxylic acid compound and also a metabolite of Isoniazid (HY-B0329). Derivatives of Isonicotinic acid exhibit antiviral activity against influenza viruses.
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HY-N0216R
Benzoic acid (Standard) 99.73% Benzoic acid (Standard) is the analytical standard of Benzoic acid. This product is intended for research and analytical applications. Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi.
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HY-N0216S1
Benzoic acid-13C6 99.66% Benzoic acid-13C6 is the 13C-labeled Benzoic acid. Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi.
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HY-N0216S2
Benzoic acid-13C 98% Benzoic acid-13C is the 13C-labeled Benzoic acid. Benzoic acid is an aromatic alcohol existing naturally in many plants and is a common additive to food, drinks, cosmetics and other products. It acts as preservatives through inhibiting both bacteria and fungi.
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HY-N0216S6
Benzoic acid-13C7 Benzoic acid-13C7 is the 13C-labeled Benzoic acid (HY-N0216). Benzoic acid is an aromatic alcohol existing naturally in many?plants?and is a common additive to food, drinks, cosmetics and?other?products. It acts as?preservatives?through inhibiting both?bacteria?and?fungi.
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HY-W004615
Thiophene-3-carboxylic acid 99.90% Thiophene-3-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-W007708
3-Furanmethanol 99.81% 3-Furanmethanol, a volatile furan compound, can be detected in malt beverages fermented with Bifidobacterium breve. 3-Furanmethanol exhibits roasty, popcorn-like flavors.
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HY-W012946
2-Furoic acid 99.98% 2-Furoic acid (Furan-2-carboxylic acid) is an organic compound produced through furfural oxidation. 2-Furoic acid exhibits hypolipidemic effet, lowers both serum cholesterol and serum triglyceride levels in rats.
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References