(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
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
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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