tert-Butyl (4-((3-bromobenzyl)amino)-4-oxobutyl)carbamate
97%
- Product Code: 113265
CAS:
1671088-98-4
| Molecular Weight: | 371.27 g./mol | Molecular Formula: | C₁₆H₂₃BrN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30502869 | |
| Melting Point: | Boiling Point: | 547.0±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿873.00 |
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| 0.250 | 10-20 days | ฿1,737.00 |
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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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