(2R,3R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid

Reagent Code: #229548
fingerprint
CAS Number 1182366-72-8

science Other reagents with same CAS 1182366-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.7 g/mol
Formula C₁₂H₁₃ClN₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of DPP-4 inhibitors for the treatment of type 2 diabetes. Its structural features, including hydroxy and carboxylic acid groups, enhance water solubility and allow for selective binding to specific enzyme active sites, improving the efficacy of drug candidates with low side effects. The compound's stereochemistry plays a critical role in biological activity, making it valuable in producing enantiomerically pure drugs. It is also employed in research settings to explore structure-activity relationships in medicinal chemistry programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿19,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2R,3R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid
No image available

Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of DPP-4 inhibitors for the treatment of type 2 diabetes. Its structural features, including hydroxy and carboxylic acid groups, enhance water solubility and allow for selective binding to specific enzyme active sites, improving the efficacy of drug candidates with low side effects. The compound's stereochemistry plays a critical role in biological activity, making it valuable in producing enanti

Used as a key intermediate in the synthesis of certain pharmaceutical agents, particularly in the development of DPP-4 inhibitors for the treatment of type 2 diabetes. Its structural features, including hydroxy and carboxylic acid groups, enhance water solubility and allow for selective binding to specific enzyme active sites, improving the efficacy of drug candidates with low side effects. The compound's stereochemistry plays a critical role in biological activity, making it valuable in producing enantiomerically pure drugs. It is also employed in research settings to explore structure-activity relationships in medicinal chemistry programs.

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...