tert-Butyl 2-((4S,6S)-6-(cyanomethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate

95%

Reagent Code: #233414
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CAS Number 196085-85-5

science Other reagents with same CAS 196085-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.34 g/mol
Formula C₁₄H₂₃NO₄
badge Registry Numbers
MDL Number MFCD16293803
thermostat Physical Properties
Melting Point 53-55 °C
Boiling Point 364.1±17.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.016±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic agents such as DPP-4 inhibitors. Its structure, featuring a chiral 1,3-dioxane ring with cyanomethyl and tert-butyl acetate substituents, allows for selective functionalization and protection of functional groups, making it valuable in constructing complex molecules with chiral centers. Commonly employed in multi-step organic syntheses, especially in the development of protease inhibitors and other bioactive compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,560.00
inventory 50mg
10-20 days ฿27,930.00

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tert-Butyl 2-((4S,6S)-6-(cyanomethyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic agents such as DPP-4 inhibitors. Its structure, featuring a chiral 1,3-dioxane ring with cyanomethyl and tert-butyl acetate substituents, allows for selective functionalization and protection of functional groups, making it valuable in constructing complex molecules with chiral centers. Commonly employed in multi-step organic syntheses, especially in the development of protease inhibitors and other

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic agents such as DPP-4 inhibitors. Its structure, featuring a chiral 1,3-dioxane ring with cyanomethyl and tert-butyl acetate substituents, allows for selective functionalization and protection of functional groups, making it valuable in constructing complex molecules with chiral centers. Commonly employed in multi-step organic syntheses, especially in the development of protease inhibitors and other bioactive compounds.

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