CAS 5962-13-0

N-(2-Furanylmethyl)urea

Description:

N-(2-Furanylmethyl)urea, with the CAS number 5962-13-0, is an organic compound characterized by the presence of a urea functional group and a furan ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents, reflecting its polar nature due to the urea moiety. The furan ring contributes to its aromatic properties, which can influence its reactivity and interactions with other chemical species. N-(2-Furanylmethyl)urea may exhibit biological activity, making it of interest in pharmaceutical and agricultural research. Its structure allows for potential hydrogen bonding, which can affect its stability and solubility. Additionally, the compound may undergo various chemical reactions, such as nucleophilic substitutions or cycloadditions, due to the reactivity of the furan ring. Overall, N-(2-Furanylmethyl)urea is a compound of interest in organic synthesis and medicinal chemistry, with potential applications in drug development and agrochemicals.

Formula: C₆H₈N₂O₂

InChI: InChI=1S/C6H8N2O2/c7-6(9)8-4-5-2-1-3-10-5/h1-3H,4H2,(H3,7,8,9)

InChI key: InChIKey=AUHRREWMYVOMRT-UHFFFAOYSA-N

SMILES: C(NC(N)=O)C1=CC=CO1

Synonyms:

• 1-(2-Furylmethyl)urea
• 2-(Ureidomethyl)furan
• 2-Furanmethanamine, N-(aminocarbonyl)-
• Furan-2-ylmethyl-urea
• Furfurylurea
• N-(2-Furanylmethyl)urea
• N-Carbamoylfurfurylamine
• Urea, (2-furanylmethyl)-
• Urea, furfuryl-
• [(Furan-2-yl)methyl]urea
• urea, N-(2-furanylmethyl)-

Furan-2-ylmethyl-urea

CAS: 5962-13-0

Formula: C₆H₈N₂O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 140.1399

Ref: IN-DA00EW4C

N-(2-furylmethyl)urea

CAS: 5962-13-0

N-(2-furylmethyl)urea

Purity: 95%

Ref: 54-OR26756

[(furan-2-yl)methyl]urea

CAS: 5962-13-0

Purity: ≥97%

Molecular weight: 140.1419983

Ref: 10-F642778

[(Furan-2-yl)methyl]urea

CAS: 5962-13-0

[(Furan-2-yl)methyl]urea (FMU) is a urea derivative that has been synthesized to inhibit cholesterol acyltransferase (CAT). This enzyme is responsible for the synthesis of lipoproteins, which are involved in the transport and storage of cholesterol. FMU inhibits CAT by forming a covalent bond with the catalytic cysteine residue, thereby inhibiting its activity. FMU also has an activating effect on staphylococcus, which may be due to its ability to inhibit bacterial amines. It also has an inhibitory effect on platelets, which may be due to its ability to bind to the surface of these cells.

Formula: C₆H₈N₂O₂

Purity: Min. 95%

Molecular weight: 140.14 g/mol

Ref: 3D-FAA96213