CAS 17377-95-6

Benzylanisidine

Description:

Benzylanisidine, with the CAS number 17377-95-6, is an organic compound that features both an aniline and an anisole structure, making it a member of the substituted aniline family. It typically appears as a solid and is characterized by its aromatic properties due to the presence of benzene rings. The compound is known for its potential applications in organic synthesis, particularly in the production of dyes, pharmaceuticals, and agrochemicals. Its molecular structure includes a benzyl group attached to an anisidine moiety, which contributes to its reactivity and solubility in organic solvents. Benzylanisidine may exhibit moderate toxicity, and safety precautions should be taken when handling it, as with many aromatic amines. Additionally, it may undergo various chemical reactions, such as electrophilic substitution, due to the electron-donating nature of the methoxy group in the anisidine part of the molecule. Overall, benzylanisidine is a versatile compound with significant relevance in chemical research and industrial applications.

Formula: C₁₄H₁₅NO

InChI: InChI=1/C14H15NO/c1-16-14-9-7-13(8-10-14)15-11-12-5-3-2-4-6-12/h2-10,15H,11H2,1H3

SMILES: COc1ccc(cc1)NCc1ccccc1

Synonyms:

• N-Benzyl-4-anisidine
• N-Benzyl-4-methoxyaniline

N-Benzyl-p-anisidine

CAS: 17377-95-6

Formula: C₁₄H₁₅NO

Purity: >98.0%(GC)(T)

Color and Shape: Light yellow to Brown powder to crystal

Molecular weight: 213.28

Ref: 3B-B0409

BENZENEMETHANAMINE, N-(4-METHOXYPHENYL)-

CAS: 17377-95-6

Formula: C₁₄H₁₅NO

Purity: 95%

Color and Shape: Solid

Molecular weight: 213.2750

Ref: IN-DA001Z6I

N-Benzyl-4-methoxyaniline

CAS: 17377-95-6

N-Benzyl-4-methoxyaniline

Purity: 98%

Molecular weight: 213.28g/mol

Ref: 54-OR95675

N-Benzyl-4-methoxyaniline

CAS: 17377-95-6

Purity: 95%

Molecular weight: 213.2799988

Ref: 10-F606485

N-Benzyl-4-methoxyaniline

CAS: 17377-95-6

N-Benzyl-4-methoxyaniline is an organic compound that is used in the manufacture of dyes and pharmaceuticals. This chemical has been shown to be a substrate for glutamate dehydrogenase, which is an enzyme that converts it into 2,3-dihydroxyphenylalanine (DOPA). N-Benzyl-4-methoxyaniline also reacts with trifluoroacetic acid, generating benzaldehyde. The reaction mechanism of this molecule is nucleophilic attack by the hydroxyl group on the benzene ring.
The detection sensitivity of this compound was improved through x-ray crystal structures and FTIR spectroscopy studies. It has been shown to have a m2 phenotype, which is associated with cancer.

Formula: C₁₄H₁₅NO

Purity: Min. 95%

Molecular weight: 213.28 g/mol

Ref: 3D-SAA37795