(R)-2-Amino-2-(furan-2-yl)ethan-1-ol hydrochloride

95%

Reagent Code: #229249
fingerprint
CAS Number 2829279-63-0

science Other reagents with same CAS 2829279-63-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.6 g/mol
Formula C₆H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD12760072
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and antiviral agents. Its structural features make it valuable in asymmetric synthesis, where the chiral center contributes to stereoselective reactions. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the presence of both amino and hydroxyl functional groups, which can interact with biological targets. Also utilized in medicinal chemistry for optimizing drug candidates requiring furan-containing moieties with enhanced solubility and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,360.00
250mg
10-20 days ฿21,000.00
(R)-2-Amino-2-(furan-2-yl)ethan-1-ol hydrochloride
No image available

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and antiviral agents. Its structural features make it valuable in asymmetric synthesis, where the chiral center contributes to stereoselective reactions. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the presence of both amino and hydroxyl functional groups, which can interact with biological targets. Also utilized in medicinal

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of bioactive molecules and antiviral agents. Its structural features make it valuable in asymmetric synthesis, where the chiral center contributes to stereoselective reactions. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to the presence of both amino and hydroxyl functional groups, which can interact with biological targets. Also utilized in medicinal chemistry for optimizing drug candidates requiring furan-containing moieties with enhanced solubility and binding affinity.

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...