(S)-Benzo[d]thiazol-2-ylmethyl 2-(2-fluorophenylsulfonamido)propanoate

98%

Reagent Code: #233199
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CAS Number 956731-22-9

science Other reagents with same CAS 956731-22-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 394.44 g/mol
Formula C₁₇H₁₅FN₂O₄S₂
badge Registry Numbers
MDL Number MFCD08487178
thermostat Physical Properties
Boiling Point 556.6±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.433±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of chiral pharmaceuticals. Its structure supports the creation of stereoselective sulfonamide-based agents, which are relevant in medicinal chemistry for targeting enzymes and receptors. Commonly employed in research settings to design protease inhibitors and anti-inflammatory agents. Also utilized in asymmetric synthesis due to the chiral center, enabling the production of enantiomerically pure drugs. Shows potential in agrochemical research for developing new active ingredients with improved selectivity and environmental profiles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,200.00
inventory 100mg
10-20 days ฿15,640.00
(S)-Benzo[d]thiazol-2-ylmethyl 2-(2-fluorophenylsulfonamido)propanoate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of chiral pharmaceuticals. Its structure supports the creation of stereoselective sulfonamide-based agents, which are relevant in medicinal chemistry for targeting enzymes and receptors. Commonly employed in research settings to design protease inhibitors and anti-inflammatory agents. Also utilized in asymmetric synthesis due to the chiral center, enabling the production of enantiomerically pure drugs.
Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of chiral pharmaceuticals. Its structure supports the creation of stereoselective sulfonamide-based agents, which are relevant in medicinal chemistry for targeting enzymes and receptors. Commonly employed in research settings to design protease inhibitors and anti-inflammatory agents. Also utilized in asymmetric synthesis due to the chiral center, enabling the production of enantiomerically pure drugs. Shows potential in agrochemical research for developing new active ingredients with improved selectivity and environmental profiles.
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