rel-(3aS,6aS)-Hexahydro-2H-thieno[2,3-c]pyrrole 1,1-dioxide hydrochloride

97%

Reagent Code: #233181
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CAS Number 1320326-61-1

science Other reagents with same CAS 1320326-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.68 g/mol
Formula C₆H₁₂ClNO₂S
thermostat Physical Properties
Melting Point >200 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid, bicyclic structure with a sulfonamide group makes it valuable for designing enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also utilized in asymmetric synthesis and catalysis as a scaffold for chiral auxiliaries or ligands.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,960.00
inventory 250mg
10-20 days ฿25,320.00

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rel-(3aS,6aS)-Hexahydro-2H-thieno[2,3-c]pyrrole 1,1-dioxide hydrochloride
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Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid, bicyclic structure with a sulfonamide group makes it valuable for designing enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also utilized in asymme
Used in organic synthesis as a chiral building block for pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid, bicyclic structure with a sulfonamide group makes it valuable for designing enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide motifs while offering improved metabolic stability. Also utilized in asymmetric synthesis and catalysis as a scaffold for chiral auxiliaries or ligands.
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