tert-Butyl (3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)carbamate

95%

  • Product Code: 85286
  CAS:    1638765-26-0
Molecular Weight: 213.27 g./mol Molecular Formula: C₁₁H₁₉NO₃
EC Number: MDL Number: MFCD27987007
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, keep away from light, dry and sealed
Product Description: This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring a bicyclo[1.1.1]pentane core, is valuable for creating rigid, three-dimensional frameworks that can enhance the potency and selectivity of drug candidates. Additionally, the tert-butyl carbamate group provides a protective function for amines during multi-step synthetic processes, ensuring stability and controlled reactivity. This compound is often employed in medicinal chemistry to explore novel therapeutic agents, particularly in areas such as central nervous system disorders and enzyme inhibition studies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿5,400.00
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-
0.250 10-20 days ฿9,900.00
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-
1.000 10-20 days ฿20,790.00
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tert-Butyl (3-(hydroxymethyl)bicyclo[1.1.1]pentan-1-yl)carbamate
This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the synthesis of biologically active compounds. Its structure, featuring a bicyclo[1.1.1]pentane core, is valuable for creating rigid, three-dimensional frameworks that can enhance the potency and selectivity of drug candidates. Additionally, the tert-butyl carbamate group provides a protective function for amines during multi-step synthetic processes, ensuring stability and controlled reactivity. This compound is often employed in medicinal chemistry to explore novel therapeutic agents, particularly in areas such as central nervous system disorders and enzyme inhibition studies.
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