N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester

95%

  • Product Code: 51151
  CAS:    338990-31-1
Molecular Weight: 415.86 g./mol Molecular Formula: C₁₈H₂₆ClN₃O₆
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily utilized in the synthesis of prodrugs, particularly in the development of targeted drug delivery systems. Its structure allows it to act as a protective group for amines, enabling controlled release of active pharmaceutical ingredients in specific physiological conditions. It is often employed in the design of anticancer agents, where it helps improve the selectivity and efficacy of the drugs by releasing the active compound in tumor tissues. Additionally, it finds application in peptide chemistry for the protection of amino groups during complex synthetic processes. Its chloroethyl ester group is key to its role as a prodrug linker, facilitating the release of therapeutic agents under specific enzymatic or chemical conditions.
Product Specification:
Test Specification
APPEARANCE Yellow Liquid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿390.00
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1.000 10-20 days ฿980.00
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5.000 10-20 days ฿3,210.00
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-
25.000 10-20 days ฿10,710.00
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-
N-Methyl-N-(3-[((N-tert-butoxycarbonyl-N-methylamino)acetoxy)methyl]pyridin-2-yl)carbamic acid 1-chloroethyl ester
This chemical is primarily utilized in the synthesis of prodrugs, particularly in the development of targeted drug delivery systems. Its structure allows it to act as a protective group for amines, enabling controlled release of active pharmaceutical ingredients in specific physiological conditions. It is often employed in the design of anticancer agents, where it helps improve the selectivity and efficacy of the drugs by releasing the active compound in tumor tissues. Additionally, it finds application in peptide chemistry for the protection of amino groups during complex synthetic processes. Its chloroethyl ester group is key to its role as a prodrug linker, facilitating the release of therapeutic agents under specific enzymatic or chemical conditions.
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