2-MEthylsulfanyl-5,6,7,9-Tetrahydro-Pyrimido[5,4-E][1,4]Diazepine-8-Carboxylic Acid Tert-Butyl Ester
≥95%
- Product Code: 87303
CAS:
1251000-26-6
Molecular Weight: | 296.39 g./mol | Molecular Formula: | C₁₃H₂₀N₄O₂S |
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EC Number: | MDL Number: | MFCD14581561 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure makes it valuable for constructing heterocyclic compounds, which are often explored for their potential biological activities. Researchers investigate its use in designing drugs targeting neurological disorders, given its diazepine moiety, which is commonly associated with central nervous system activity. Additionally, it may serve as a building block in the development of enzyme inhibitors or receptor modulators, contributing to advancements in medicinal chemistry. Its tert-butyl ester group enhances stability during synthetic processes, making it a practical choice for multi-step organic reactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.001 | 10-20 days | ฿4,437.00 |
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0.005 | 10-20 days | ฿7,578.00 |
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2-MEthylsulfanyl-5,6,7,9-Tetrahydro-Pyrimido[5,4-E][1,4]Diazepine-8-Carboxylic Acid Tert-Butyl Ester
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure makes it valuable for constructing heterocyclic compounds, which are often explored for their potential biological activities. Researchers investigate its use in designing drugs targeting neurological disorders, given its diazepine moiety, which is commonly associated with central nervous system activity. Additionally, it may serve as a building block in the development of enzyme inhibitors or receptor modulators, contributing to advancements in medicinal chemistry. Its tert-butyl ester group enhances stability during synthetic processes, making it a practical choice for multi-step organic reactions.
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