13509-75-6

Usage

Uses

Used in Pharmaceutical and Industrial Compounds:
Benzenemethanamine, .alpha.-butyl-N-methylis used as an intermediate or precursor in the synthesis of various pharmaceutical and industrial compounds due to its versatile chemical properties.
Used in Corrosion Inhibition:
Benzenemethanamine, .alpha.-butyl-N-methylis used as a corrosion inhibitor, helping to prevent the degradation of materials in various industrial applications.
Used in Antioxidant Applications:
Benzenemethanamine, .alpha.-butyl-N-methylis used as an antioxidant, protecting materials from oxidative damage and extending their lifespan.
Used in Rubber and Plastic Production:
Benzenemethanamine, .alpha.-butyl-N-methylis used as an ingredient in the production of rubber and plastic materials, contributing to their properties and performance.
Used in Polymer Manufacturing:
Benzenemethanamine, .alpha.-butyl-N-methylis used as a stabilizer in the manufacturing of different types of polymers, enhancing their stability and performance.
Safety Precautions:
It is important to handle Benzenemethanamine, .alpha.-butyl-N-methylwith care, as it can be harmful if ingested, inhaled, or comes into contact with the skin or eyes. Proper safety measures should be taken during its use and storage to minimize potential risks.

Upstream product

• 693-03-8 n-butyl magnesium bromide 
• 622-29-7 N-Benzylidenemethylamine 
• 88070-48-8 N-methylbenzamide 
• 542-69-8 1-iodo-butane 
• 109-72-8 n-butyllithium 
• 51029-13-1 N-benzyl-N-methyl triflamide 

Relevant academic research and scientific papers

A general method for the one-pot reductive functionalization of secondary amides

A one-pot reaction for the transformation of common secondary amides into amines with C-C bond formation is described. This method consists of in situ amide activation with Tf2O-partial reduction-addition of C-nucleophiles. The method is general in scope, which allows employing both hard nucleophiles (RMgX, RLi) and soft nucleophiles, as well as enolates. With the use of soft nucleophiles, the reaction proceeded with high chemoselectivity at a secondary amide in the presence of ester, cyano, nitro, and tertiary amide groups.

Direct transformation of secondary amides into secondary amines: Triflic anhydride activated reductive alkylation

Versatile and mild: The first general method for the title transformation has been developed (see scheme; 2-F-Py=2-fluoropyridine; Tf=trifluorosulfonyl). The amines are synthesized in good yields and the ketimine intermediates can be isolated before the r

The chemistry of alkylstrontium halide analogues: Barbier-type alkylation of imines with alkyl halides

The chemistry of alkylstrontium halide analogues was examined. In the presence of metallic strontium, the Barbier-type alkylation of imines with alkyl iodides proceeded smoothly at room temperature under an argon atmosphere to afford the corresponding alk

Triflamides: Elimination of the triflyl anion versus substitution of the trifluoromethide group

Base-induced elimination of CF3SO2- and nucleophilic substitution of CF3- were observed in the reaction of secondary triflamides with alkyllithium reagents.