91552-82-8

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is used as a raw material for the production of various pharmaceuticals and organic compounds. Its unique structure and properties make it a valuable component in the synthesis of new drugs and medicinal agents.
Used in Organic Synthesis:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is used as a building block in organic synthesis for creating a range of organic compounds. Its versatility in forming different chemical bonds and its stability contribute to its utility in this field.
Used in Research and Development:
2-(4-TERT-BUTYLPHENYL)ETHYLAMINE is utilized in research and development applications, where its properties are explored for potential new uses and to enhance existing processes in chemical and pharmaceutical research.

Upstream product

• 3288-99-1 4-tert-butylbenzyl cyanide 
• 100368-57-8 2-(4-(tert-butyl)phenyl)acetamide 
• 1746-23-2 4-tert-Butylstyrene 
• 32857-63-9 4-t-butylphenylacetic acid 
• 3549-23-3 methyl 2-(4-tert-butylphenyl)acetate 

Downstream Products

• 184003-55-2 1-tert-butyl-4-(2-isothiocyanatoethyl)benzene 
• 274914-89-5 3-[2-(4-tert-Butyl-phenyl)-ethylamino]-4-(4-methoxy-phenyl)-cyclobut-3-ene-1,2-dione 
• 134999-96-5 4-[2-[4-(t-butyl)phenyl]ethylamino]pyrido-[4,3-d]pyrimidine 
• 1067904-10-2 C₂₀H₂₄N₂O₃S 
• 134531-77-4 N-[2-[4-(t-butyl)phenyl]ethyl]-1,5-naphthyridin-4-amine 
• 184003-56-3 1-[2-(4-tert-Butyl-phenyl)-ethyl]-3-{4-[2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-ethoxy]-3-methoxy-benzyl}-thiourea 

Relevant academic research and scientific papers

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

PROCESS FOR PRODUCING DIHYDROISOQUINOLINE ZWITTERIONS

This invention relates to a preparation of zwitterionic sulfates of substituted or unsubstituted 3, 4-dihydroisoquinoline.