2978-60-1

Usage

Uses

Used in Pharmaceutical Industry:
2-Methylbut-3-en-2-amine is used as a key intermediate in the synthesis of naphthyridine derivatives, which are known for their cholesterol acyltransferase inhibitory properties. These derivatives are valuable in the development of drugs targeting high cholesterol levels and related cardiovascular diseases.
Used in Chemical Synthesis:
In the chemical industry, 2-methylbut-3-en-2-amine serves as a versatile building block for the creation of various compounds with diverse applications. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of specialty chemicals, agrochemicals, and other industrial products.

Upstream product

• 2978-58-7 1,1-dimethylprop-3-ynylamine 
• 91989-80-9 N-<3-(3-methyl-1-butenyl)> trichloroacetamide 
• 959624-01-2 1-(diphenylmethylene)-2-(2-methylbut-3-en-2-yl)hydrazine 
• 959624-09-0 O-benzyl-N-(2-methylbut-3-en-2-yl)hydroxylamine 
• 1111-97-3 3-chloro-3-methylbut-1-yne 
• 7472-48-2 2,2-dimethyl-but-3-enoic acid amide 

Downstream Products

• 594-39-8 2-methyl-2-butylamine 
• 100384-75-6 1-cyclo-hexyl-3-(1,1-dimethylallyl)-thiourea 
• 41809-44-3 (1,1-dimethylallyl)phenyldiazene 
• 1191-16-8 3-methylbut-2-enyl acetate 
• 24509-88-4 2-methyl-3-buten-2-yl acetate 
• 2809-97-4 N-<1.1-Dimethyl-allyl>-1.1-dimethyl-propargyl-amin 

Relevant academic research and scientific papers

Primary tert- and sec-allylamines via palladium-catalyzed hydroamination and allylic substitution with hydrazine and hydroxylamine derivatives

(Chemical Equation Presented) Amines of control: Palladium-catalyzed reactions of hydrazine and hydroxylamine derivatives with dienes and allylic esters form products from C-N bond formation at the more substituted position of the allyl intermediate with

Palladium-catalysed N-annulation routes to indoles: The synthesis of indoles with sterically demanding N-substituents, including demethylasterriquinone A1

Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of indoles bearing sterically demanding N-substituents, including the natural product demethylasterriquinone A1. The Royal Society of Chemistry.

Methods and compositions for treating amyloid-related diseases

Methods, compounds, pharmaceutical compositions and kits are described for treating or preventing amyloid-related disease.