tert-Butyl (4-((3-bromobenzyl)amino)-4-oxobutyl)carbamate

97%

Reagent Code: #113265
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CAS Number 1671088-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 371.27 g/mol
Formula C₁₆H₂₃BrN₂O₃
badge Registry Numbers
MDL Number MFCD30502869
thermostat Physical Properties
Boiling Point 547.0±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as an intermediate in the development of biologically active compounds, particularly in the synthesis of small molecules that target specific proteins or enzymes. Its structure, featuring a bromobenzyl group and a carbamate moiety, makes it valuable for constructing complex molecules with potential therapeutic applications. Researchers often employ it in drug discovery projects, where it can be incorporated into larger molecules to enhance binding affinity or modify pharmacokinetic properties. Additionally, it may be used in the preparation of peptide analogs or inhibitors, contributing to the study of biochemical pathways and disease mechanisms. Its versatility in chemical reactions, such as amide bond formation or cross-coupling, further expands its utility in medicinal chemistry and material science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿873.00
inventory 250mg
10-20 days ฿1,737.00
tert-Butyl (4-((3-bromobenzyl)amino)-4-oxobutyl)carbamate
This chemical is primarily used in organic synthesis and pharmaceutical research. It serves as an intermediate in the development of biologically active compounds, particularly in the synthesis of small molecules that target specific proteins or enzymes. Its structure, featuring a bromobenzyl group and a carbamate moiety, makes it valuable for constructing complex molecules with potential therapeutic applications. Researchers often employ it in drug discovery projects, where it can be incorporated into larger molecules to enhance binding affinity or modify pharmacokinetic properties. Additionally, it may be used in the preparation of peptide analogs or inhibitors, contributing to the study of biochemical pathways and disease mechanisms. Its versatility in chemical reactions, such as amide bond formation or cross-coupling, further expands its utility in medicinal chemistry and material science.
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