(S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate
97%
- Product Code: 60156
CAS:
1187929-79-8
Molecular Weight: | 216.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₃ |
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EC Number: | MDL Number: | MFCD06796250 | |
Melting Point: | Boiling Point: | 311°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both morpholine and tert-butyl carboxylate groups, makes it a valuable building block for designing drugs, particularly those targeting neurological and cardiovascular diseases. It is often employed in the development of enzyme inhibitors and receptor modulators due to its ability to interact with specific biological targets. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is critical in optimizing drug efficacy and reducing side effects. Researchers also use it in medicinal chemistry studies to explore structure-activity relationships and improve drug candidates' pharmacokinetic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿4,779.00 |
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0.250 | 10-20 days | ฿7,461.00 |
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1.000 | 10-20 days | ฿19,098.00 |
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(S)-tert-Butyl 3-(aminomethyl)morpholine-4-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring both morpholine and tert-butyl carboxylate groups, makes it a valuable building block for designing drugs, particularly those targeting neurological and cardiovascular diseases. It is often employed in the development of enzyme inhibitors and receptor modulators due to its ability to interact with specific biological targets. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is critical in optimizing drug efficacy and reducing side effects. Researchers also use it in medicinal chemistry studies to explore structure-activity relationships and improve drug candidates' pharmacokinetic properties.
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