1-(2,2,2-Trifluoroacetyl)piperidine-4-carboxylic acid

97%

  • Product Code: 114278
  CAS:    126501-70-0
Molecular Weight: 225.17 g./mol Molecular Formula: C₈H₁₀F₃NO₃
EC Number: MDL Number: MFCD03840837
Melting Point: Boiling Point: 386.6°C at 760 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: 1-(2,2,2-Trifluoroacetyl)piperidine-4-carboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various pharmacologically active compounds. Its structure, featuring a trifluoroacetyl group and a carboxylic acid moiety, makes it valuable for modifying and enhancing the properties of drug candidates. This chemical is often employed in the synthesis of piperidine derivatives, which are commonly found in medications targeting the central nervous system, such as antipsychotics and analgesics. Additionally, its trifluoroacetyl group can act as a protecting group in peptide synthesis, enabling the selective modification of amino acids during the production of complex peptides. In medicinal chemistry, it is utilized to create molecules with improved metabolic stability and bioavailability, as the trifluoroacetyl group can influence the pharmacokinetic properties of the resulting compounds. Researchers also leverage its reactivity to develop novel inhibitors for enzymes or receptors, contributing to the discovery of new therapeutic agents.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿783.00
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0.250 10-20 days ฿1,197.00
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1.000 10-20 days ฿2,916.00
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5.000 10-20 days ฿11,574.00
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1-(2,2,2-Trifluoroacetyl)piperidine-4-carboxylic acid
1-(2,2,2-Trifluoroacetyl)piperidine-4-carboxylic acid is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various pharmacologically active compounds. Its structure, featuring a trifluoroacetyl group and a carboxylic acid moiety, makes it valuable for modifying and enhancing the properties of drug candidates. This chemical is often employed in the synthesis of piperidine derivatives, which are commonly found in medications targeting the central nervous system, such as antipsychotics and analgesics. Additionally, its trifluoroacetyl group can act as a protecting group in peptide synthesis, enabling the selective modification of amino acids during the production of complex peptides. In medicinal chemistry, it is utilized to create molecules with improved metabolic stability and bioavailability, as the trifluoroacetyl group can influence the pharmacokinetic properties of the resulting compounds. Researchers also leverage its reactivity to develop novel inhibitors for enzymes or receptors, contributing to the discovery of new therapeutic agents.
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