Tert-butyl (3-(hydroxymethyl)-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyridin-6-yl)carbamate
95%
- Product Code: 123628
CAS:
2139226-14-3
Molecular Weight: | 268.31 g./mol | Molecular Formula: | C₁₂H₂₀N₄O₃ |
---|---|---|---|
EC Number: | MDL Number: | MFCD28390423 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic compounds. Its structure is particularly valuable in the creation of heterocyclic molecules, which are often explored for their potential therapeutic properties. It is frequently employed in the preparation of compounds targeting neurological disorders, due to its ability to interact with specific receptors in the brain. Additionally, its reactive functional groups make it a versatile building block in medicinal chemistry, enabling the development of novel drugs with enhanced efficacy and selectivity. Researchers also leverage its properties in the design of prodrugs, which are biologically inactive compounds that convert into active drugs within the body. Its application extends to the study of enzyme inhibition, where it serves as a scaffold for designing inhibitors that modulate biochemical pathways.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.100 | 10-20 days | ฿18,000.00 |
+
-
|
Tert-butyl (3-(hydroxymethyl)-4,5,6,7-tetrahydro-[1,2,3]triazolo[1,5-a]pyridin-6-yl)carbamate
This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic compounds. Its structure is particularly valuable in the creation of heterocyclic molecules, which are often explored for their potential therapeutic properties. It is frequently employed in the preparation of compounds targeting neurological disorders, due to its ability to interact with specific receptors in the brain. Additionally, its reactive functional groups make it a versatile building block in medicinal chemistry, enabling the development of novel drugs with enhanced efficacy and selectivity. Researchers also leverage its properties in the design of prodrugs, which are biologically inactive compounds that convert into active drugs within the body. Its application extends to the study of enzyme inhibition, where it serves as a scaffold for designing inhibitors that modulate biochemical pathways.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :