1-Piperidinecarboxylic acid, 4-amino-3-methoxy-, 1,1-dimethylethyl ester, (3R,4S)-rel-

97%

Reagent Code: #223311
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CAS Number 1171124-68-7

science Other reagents with same CAS 1171124-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.304 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD09749826
thermostat Physical Properties
Boiling Point 306.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as certain antiviral drugs. It serves as a chiral building block in asymmetric synthesis, enabling the construction of complex molecules with high stereochemical purity. Commonly employed in the development of HIV and HCV treatments due to its ability to mimic amino acid structures and enhance metabolic stability. Also utilized in research settings for the design of enzyme inhibitors and bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,600.00
inventory 5g
10-20 days ฿35,200.00
inventory 10g
10-20 days ฿67,200.00
inventory 25g
10-20 days ฿160,000.00
1-Piperidinecarboxylic acid, 4-amino-3-methoxy-, 1,1-dimethylethyl ester, (3R,4S)-rel-
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as certain antiviral drugs. It serves as a chiral building block in asymmetric synthesis, enabling the construction of complex molecules with high stereochemical purity. Commonly employed in the development of HIV and HCV treatments due to its ability to mimic amino acid structures and enhance metabolic stability. Also utilized in research settings for the design of enzyme inhibitors an

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as certain antiviral drugs. It serves as a chiral building block in asymmetric synthesis, enabling the construction of complex molecules with high stereochemical purity. Commonly employed in the development of HIV and HCV treatments due to its ability to mimic amino acid structures and enhance metabolic stability. Also utilized in research settings for the design of enzyme inhibitors and bioactive compounds.

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