(R)-3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride

95%

Reagent Code: #230749
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CAS Number 935455-27-9

science Other reagents with same CAS 935455-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.65 g/mol
Formula C₄H₁₀ClNO₂S
badge Registry Numbers
MDL Number MFCD22418841
inventory_2 Storage & Handling
Storage Room temperature, avoid light, and inert gas storage

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its sulfone functionality and amine group allow for diverse chemical transformations, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural similarity to natural amino acids and its ability to enhance metabolic stability. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,000.00
inventory 250mg
10-20 days ฿8,000.00
inventory 1g
10-20 days ฿24,000.00
inventory 5g
10-20 days ฿88,000.00
(R)-3-Aminotetrahydrothiophene 1,1-dioxide hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its sulfone functionality and amine group allow for diverse chemical transformations, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural similarity to natural amino acids and its ability to enhanc

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its sulfone functionality and amine group allow for diverse chemical transformations, making it valuable in medicinal chemistry for constructing heterocyclic systems. Commonly employed in the preparation of enzyme inhibitors and receptor modulators due to its structural similarity to natural amino acids and its ability to enhance metabolic stability. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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