CAS 10551-58-3

5-(Acetoxymethyl)-2-furaldehyde

Description:

5-(Acetoxymethyl)-2-furaldehyde, with the CAS number 10551-58-3, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features an aldehyde functional group and an acetoxymethyl substituent, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid with a distinctive odor, indicative of its aromatic nature. The presence of the acetoxy group enhances its solubility in organic solvents and may influence its reactivity in various chemical reactions, such as nucleophilic substitutions or condensation reactions. This compound is of interest in the field of organic chemistry for its potential use in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Additionally, its derivatives may exhibit biological activity, making it a subject of research in medicinal chemistry. Proper handling and storage are essential due to its reactive nature and potential health hazards associated with aldehyde compounds.

Formula: C₈H₈O₄

InChI: InChI=1/C8H8O4/c1-6(10)11-5-8-3-2-7(4-9)12-8/h2-4H,5H2,1H3

InChI key: InChIKey=QAVITTVTXPZTSE-UHFFFAOYSA-N

SMILES: C(OC(C)=O)C=1OC(C=O)=CC1

Synonyms:

• (5-Formylfuran-2-Yl)Methyl Acetate
• 2-Furaldehyde, 5-(hydroxymethyl)-, acetate
• 2-Furancarboxaldehyde, 5-[(acetyloxy)methyl]-
• 5-(Acetoxymethyl)furfural
• 5-(Acetoxymethyl)furfuraldehyde
• 5-Acetoxymethyl-2-furancarboxaldehyde
• 5-Acetoxymethyl-2-furfural
• 5-Formyl-2-furfuryl acetate
• 5-Formyl-2-furylmethyl acetate
• 5-Formylfurfuryl Acetate
• 5-[(Acetyloxy)methyl]-2-furancarboxaldehyde
• AMF
• Acetic Acid 5-Formylfurfuryl Ester
• 5-(Acetoxymethyl)-2-furaldehyde
• 5-Acetoxymethyl-2-furaldehyde, GC 99%
• 5-ACETOXYMETHYLFURFURAL
• (5-Formyl-2-furyl)methyl acetate
• 5-Acetoxymethyl-2-furaldehyde, tech.
• 5-Acetoxymethyl-2-furaldehyde ,97%
• 5-ACETOXYMETHYL-2-FURALDEHYDE 97%

5-Acetoxymethylfurfural

CAS: 10551-58-3

Formula: C₈H₈O₄

Purity: >98.0%(GC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 168.15

Ref: 3B-A1484

(5-Formylfuran-2-yl)methyl acetate

CAS: 10551-58-3

Formula: C₈H₈O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 168.1467

Ref: IN-DA003MBO

(5-Formylfuran-2-yl)methyl acetate

CAS: 10551-58-3

(5-Formylfuran-2-yl)methyl acetate

Purity: 98%

Molecular weight: 168.15g/mol

Ref: 54-OR89950

5-Acetoxymethyl-2-furaldehyde

CAS: 10551-58-3

5-Acetoxymethyl-2-furaldehyde

Purity: 98%

Molecular weight: 168.15g/mol

Ref: 54-OR6750T

5-Acetoxymethyl-2-furaldehyde

Controlled Product

CAS: 10551-58-3

Applications Used for reduction of off-taste of vinegar.
References Chinnici, F., et al.: J. Chromatogr. Sci., 41, 305 (2003), Masino, F., et al.: Food Chem., 92, 673 (2005),

Formula: C₈H₈O₄

Color and Shape: Neat

Molecular weight: 168.15

Ref: TR-A167500

5-Acetoxymethyl-2-furaldehyde

CAS: 10551-58-3

5-Acetoxymethyl-2-furaldehyde is a furanic acid that is found in the plant Triticum aestivum. This compound has been shown to have antifungal and anticancer properties. 5-Acetoxymethyl-2-furaldehyde inhibits the growth of bacteria by forming a complex with p-hydroxybenzoic acid, which prevents the formation of amines. The toxicity of this compound may also be due to its ability to cause DNA damage, leading to cell death. 5-Acetoxymethyl-2-furaldehyde can be used as an oxidation catalyst for reactions involving amines. It can also be produced by oxidizing 2,5 furanone with hydrogen peroxide and hydrochloric acid at high temperatures. The reaction mechanism is not well understood but it is believed that 5 acetoxymethyl - 2 furaldehyde is formed from the dehydration of furfuraldehyde.

Formula: C₈H₈O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 168.15 g/mol

Ref: 3D-FA05450

5-(Acetoxymethyl)furfural

CAS: 10551-58-3

Formula: C₈H₈O₄

Purity: 97%

Molecular weight: 168.148

Ref: 10-F223769