CAS 568577-84-4

1-(4-ethylphenyl)-N-methylmethanamine

Description:

1-(4-Ethylphenyl)-N-methylmethanamine, identified by its CAS number 568577-84-4, is an organic compound characterized by its amine functional group. This substance features a methyl group attached to a methanamine backbone, along with a 4-ethylphenyl substituent, which contributes to its hydrophobic properties. The presence of the ethyl group on the phenyl ring enhances its steric bulk and can influence its reactivity and interaction with biological systems. Typically, compounds of this nature may exhibit properties such as moderate solubility in organic solvents and limited solubility in water, owing to their hydrophobic characteristics. Additionally, the compound may participate in various chemical reactions typical of amines, such as alkylation and acylation. Its potential applications could span across pharmaceuticals, agrochemicals, or as intermediates in organic synthesis, although specific uses would depend on further research into its biological activity and safety profile. As with all chemical substances, handling should be conducted with appropriate safety measures in place.

Formula: C₁₀H₁₅N

InChI: InChI=1/C10H15N/c1-3-9-4-6-10(7-5-9)8-11-2/h4-7,11H,3,8H2,1-2H3

SMILES: CCc1ccc(cc1)CNC

Synonyms:

• Benzenemethanamine, 4-ethyl-N-methyl-
• N-(4-ethylbenzyl)-N-methylamine
• 4-Ethyl-N-methyl-benzylamine
• 1-(4-Ethylphenyl)-N-methylmethanamine

1-(4-Ethylphenyl)-N-methylmethanamine

CAS: 568577-84-4

Formula: C₁₀H₁₅N

Purity: 98%

Color and Shape: Liquid

Molecular weight: 149.2328

Ref: IN-DA003T6U

N-(4-Ethylbenzyl)-N-methylamine

CAS: 568577-84-4

N-(4-Ethylbenzyl)-N-methylamine

Purity: 95%

Molecular weight: 149.23g/mol

Ref: 54-OR952845

(4-ethylbenzyl)methylamine

CAS: 568577-84-4

Formula: C₁₀H₁₅N

Purity: 98%

Color and Shape: Liquid

Molecular weight: 149.237

Ref: 10-F308500

N-(4-Ethylbenzyl)-n-methylamine

CAS: 568577-84-4

N-(4-Ethylbenzyl)-n-methylamine is a biodegradable, low temperature, and catalytic process for the production of methylamines from acetonitrile. The reaction mechanism of this process is based on the hydrosilylation of acetone with anions such as chloride or bromide. This process has a high selectivity and does not produce by-products such as carbon dioxide or hydrogen cyanide. The reaction can be performed at room temperature and is able to operate at low temperatures without requiring expensive equipment.

Formula: C₁₀H₁₅N

Purity: Min. 95%

Molecular weight: 149.24 g/mol

Ref: 3D-TXA57784