(3R,4R)-4-Azidopiperidin-3-ol

95%

Reagent Code: #232155
fingerprint
CAS Number 859854-78-7

science Other reagents with same CAS 859854-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.16 g/mol
Formula C₅H₁₀N₄O
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antiviral and neurological drugs. Its functional groups—azide and hydroxyl—allow for selective chemical modifications, including click chemistry via azide-alkyne cycloaddition, enabling efficient linkage to other molecular scaffolds. Commonly employed in medicinal chemistry for building chiral piperidine derivatives, which are prevalent in bioactive molecules. Also utilized in the preparation of protease inhibitors and receptor modulators due to its structural compatibility with enzyme active sites.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,090.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3R,4R)-4-Azidopiperidin-3-ol
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antiviral and neurological drugs. Its functional groups—azide and hydroxyl—allow for selective chemical modifications, including click chemistry via azide-alkyne cycloaddition, enabling efficient linkage to other molecular scaffolds. Commonly employed in medicinal chemistry for building chiral piperidine derivatives, which are prevalent in bioactive molecules. Also utilized i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as antiviral and neurological drugs. Its functional groups—azide and hydroxyl—allow for selective chemical modifications, including click chemistry via azide-alkyne cycloaddition, enabling efficient linkage to other molecular scaffolds. Commonly employed in medicinal chemistry for building chiral piperidine derivatives, which are prevalent in bioactive molecules. Also utilized in the preparation of protease inhibitors and receptor modulators due to its structural compatibility with enzyme active sites.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...