(S)-4-benzyl-1,3-thiazolidin-2-one

95%

Reagent Code: #235171
fingerprint
CAS Number 219821-18-8

science Other reagents with same CAS 219821-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.26 g/mol
Formula C₁₀H₁₁NOS
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and binding affinity in peptidomimetic compounds. Also utilized in the preparation of cysteine protease inhibitors due to the structural similarity with natural amino acid motifs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿46,480.00
(S)-4-benzyl-1,3-thiazolidin-2-one
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and binding affinity in peptidomimetic compounds. Also utilized in the preparation of cysteine protease inhibitors due to the structural similar

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and binding affinity in peptidomimetic compounds. Also utilized in the preparation of cysteine protease inhibitors due to the structural similarity with natural amino acid motifs.

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...