Thiomorpholinoacetic Acid 1',1'-Dioxide Monohydrate

98%

Reagent Code: #241177
fingerprint
CAS Number 155480-08-3

science Other reagents with same CAS 155480-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.22(asAnhydrous) g/mol
Formula C₆H₁₁NO₄S·H₂O
badge Registry Numbers
MDL Number MFCD00121261
thermostat Physical Properties
Melting Point 177°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antidiabetic drugs. Its structure supports the formation of stable amide bonds, making it valuable in peptide-like drug design. The sulfone group enhances solubility and metabolic stability, improving drug bioavailability. Also employed in the preparation of enzyme inhibitors due to its ability to mimic transition states in biochemical reactions. Commonly utilized in research settings for scaffold development in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 5g
10-20 days ฿5,000.00
Thiomorpholinoacetic Acid 1',1'-Dioxide Monohydrate
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antidiabetic drugs. Its structure supports the formation of stable amide bonds, making it valuable in peptide-like drug design. The sulfone group enhances solubility and metabolic stability, improving drug bioavailability. Also employed in the preparation of enzyme inhibitors due to its ability to mimic transition states in biochemical reactions. Commonly utilized in research settings

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antiviral and antidiabetic drugs. Its structure supports the formation of stable amide bonds, making it valuable in peptide-like drug design. The sulfone group enhances solubility and metabolic stability, improving drug bioavailability. Also employed in the preparation of enzyme inhibitors due to its ability to mimic transition states in biochemical reactions. Commonly utilized in research settings for scaffold development in medicinal chemistry.

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...