947661-79-2

Usage

Uses

Used in Pharmaceutical Industry:
4-[tert-butoxycarbonyl-[(4-methoxyphenyl)methyl]amino]butanoic acid is used as a drug precursor or intermediate for its potential role in the synthesis of peptide-based drugs. Its unique structural features allow for the modification of properties and functions of peptides, which can be crucial in the development of new therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-[tert-butoxycarbonyl-[(4-methoxyphenyl)methyl]amino]butanoic acid serves as a valuable chemical for exploring its pharmacological properties. The methoxy group present in its structure may confer specific characteristics that can be harnessed to enhance the effectiveness of drugs or to discover new applications in treatment and therapy.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 123-11-5 4-methoxy-benzaldehyde 
• 56-12-2 4-amino-n-butyric acid 
• 42460-98-0 4-[(4-methoxybenzyl)amino]butanoic acid 

Downstream Products

• 947661-78-1 4-[(4-methoxybenzyl)amino]butyric acid methyl ester monohydrochloride 

Relevant academic research and scientific papers

Design and synthesis of novel pyrimido[4,5-b]azepine derivatives as HER2/EGFR dual inhibitors

A novel 7,6 fused bicyclic scaffold, pyrimido[4,5-b]azepine was designed to fit into the ATP binding site of the HER2/EGFR proteins. The synthesis of this scaffold was accomplished by an intramolecular Claisen-type condensation. As the results of optimiza

FUSED HETEROCYCLIC COMPOUND

A compound of the formula: wherein ring'' A is a 7-membered or 8-membered nitrogen- containing ring optionally further substituted, ring B is an optionally substituted aryl group or an optionally substituted heteroaryl group, X1 is a group represented by -NR3-Y1-, -0-, -S-, -SO-, -SO2- or -CHR3- wherein R3 is a hydrogen atom or'' an optionally substituted aliphatic hydrocarbon group, or R3 may be bonded to the carbon atom of ring B to form an optionally substituted ring structure, and Y1 is a bond or an optionally substituted C1-4 alkylene, R1 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom or a sulfur atom, the formula = shows a single bond or a double bond, when ===R2 is - R2, R2 is a hydrogen atom, or an optionally substituted group bonded via a carbon atom, a nitrogen atom, an oxygen atom or a sulfur atom, and when ===R2 is =R2, R2 is an oxo group, an optionally substituted alkylidene group, or an optionally, substituted imino group.