(R)-2-amino-2-(2,5-dichlorophenyl)ethan-1-ol

95%

Reagent Code: #228697
fingerprint
CAS Number 1212816-55-1

science Other reagents with same CAS 1212816-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.07 g/mol
Formula C₈H₉Cl₂NO
badge Registry Numbers
MDL Number MFCD09254046
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of the triazole antifungal drug Posaconazole. Posaconazole is effective against Candida and Aspergillus species by inhibiting lanosterol 14α-demethylase, disrupting ergosterol biosynthesis essential for fungal cell membrane integrity. The (R)-stereochemistry of the compound is critical for its biological activity, making it valuable in asymmetric synthesis for pharmaceuticals. Also employed in the development of novel enzyme inhibitors due to its structural similarity to amino acid derivatives.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿39,160.00
inventory 100mg
10-20 days ฿66,560.00
(R)-2-amino-2-(2,5-dichlorophenyl)ethan-1-ol
No image available

Used as a key chiral intermediate in the synthesis of the triazole antifungal drug Posaconazole. Posaconazole is effective against Candida and Aspergillus species by inhibiting lanosterol 14α-demethylase, disrupting ergosterol biosynthesis essential for fungal cell membrane integrity. The (R)-stereochemistry of the compound is critical for its biological activity, making it valuable in asymmetric synthesis for pharmaceuticals. Also employed in the development of novel enzyme inhibitors due to its structu

Used as a key chiral intermediate in the synthesis of the triazole antifungal drug Posaconazole. Posaconazole is effective against Candida and Aspergillus species by inhibiting lanosterol 14α-demethylase, disrupting ergosterol biosynthesis essential for fungal cell membrane integrity. The (R)-stereochemistry of the compound is critical for its biological activity, making it valuable in asymmetric synthesis for pharmaceuticals. Also employed in the development of novel enzyme inhibitors due to its structural similarity to amino acid derivatives.

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...