(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-cyanopropanoate

95%

Reagent Code: #233234
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CAS Number 2703745-95-1

science Other reagents with same CAS 2703745-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.25 g/mol
Formula C₁₀H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD34187013
thermostat Physical Properties
Boiling Point 373.1±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.123±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino acids and peptidomimetic compounds. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in research and development of protease inhibitors and other bioactive molecules where structural specificity is critical. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling reactions, facilitating its incorporation into complex molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,490.00
inventory 250mg
10-20 days ฿17,140.00
(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-cyanopropanoate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino acids and peptidomimetic compounds. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in research and development of protease inhibitors and other bioactive molecules where structural specificity is critical. The Boc-protected amine and ester funct

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino acids and peptidomimetic compounds. Its stereochemistry allows for selective reactions in asymmetric synthesis, making it valuable in developing active pharmaceutical ingredients (APIs) with high enantiomeric purity. Commonly employed in research and development of protease inhibitors and other bioactive molecules where structural specificity is critical. The Boc-protected amine and ester functionalities enable stepwise deprotection and coupling reactions, facilitating its incorporation into complex molecular architectures.

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