CAS 4468-59-1

(4-Hydroxy-3-methoxyphenyl)acetonitrile

Description:

(4-Hydroxy-3-methoxyphenyl)acetonitrile, with the CAS number 4468-59-1, is an organic compound characterized by its phenolic structure, which includes a hydroxyl group (-OH) and a methoxy group (-OCH3) attached to a benzene ring. This compound features an acetonitrile functional group (-C≡N) that contributes to its reactivity and potential applications in organic synthesis. It is typically a white to off-white solid at room temperature and is soluble in polar organic solvents. The presence of the hydroxyl and methoxy groups suggests that it may exhibit antioxidant properties and could participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. Its structural features may also allow it to interact with biological systems, making it of interest in pharmaceutical research. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper safety measures are taken.

Formula: C₉H₉NO₂

InChI: InChI=1S/C9H9NO2/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,11H,4H2,1H3

InChI key: InChIKey=SDVYWMWQCJEYTC-UHFFFAOYSA-N

SMILES: O(C)C1=CC(CC#N)=CC=C1O

Synonyms:

• (4-Hydroxy-3-methoxyphenyl)acetonitrile
• 2-(4-Hydroxy-3-methoxyphenyl)acetonitrile
• 2-Methoxy-4-(cyanomethyl)phenol
• 4-Hydroxy-3-methoxybenzeneacetonitrile
• Acetonitrile, (4-hydroxy-3-methoxyphenyl)-
• Benzeneacetonitrile, 4-hydroxy-3-methoxy-
• Homovanillonitrile

2-(4-Hydroxy-3-methoxyphenyl)acetonitrile

CAS: 4468-59-1

Formula: C₉H₉NO₂

Purity: %

Color and Shape: Solid

Molecular weight: 163.1733

Ref: IN-DA003LI0

4-Hydroxy-3-methoxyphenylacetonitrile

CAS: 4468-59-1

4-Hydroxy-3-methoxyphenylacetonitrile

Formula: C₉H₉NO₂

Purity: 98+%

Color and Shape: off-white powder

Molecular weight: 163.17g/mol

Ref: 54-OR52500

(4-Hydroxy-3-methoxyphenyl)acetonitrile

CAS: 4468-59-1

Lobetyolin is a phenolic compound that has been found to be an inhibitor of monoamine oxidase. Lobetyolin is an acetylated derivative of 4-hydroxy-3-methoxyphenylacetonitrile. It has been shown to inhibit bacterial growth in vitro, with the exception of Mycobacterium tuberculosis and Mycobacterium avium complex. The optimal reaction time for lobetyolin is 3 hours at a pH between 7 and 8, with a yield of 66% at room temperature. Lobetyolin reacts rapidly with amines, alkylating them as it undergoes oxidation by hydrogen peroxide. Lobetyolin also reacts slowly with dopamine and aldehydes, but more readily with chlorides, yielding lobetyrine and chloroacetaldehyde respectively.

Formula: C₉H₉NO₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 163.17 g/mol

Ref: 3D-FH67972

4-Hydroxy-3-methoxyphenylacetonitrile

CAS: 4468-59-1

Formula: C₉H₉NO₂

Purity: 98+%

Color and Shape: Solid

Molecular weight: 163.176

Ref: 10-F146405