(R)-1,1,1-Trifluoro-N-(pyrrolidin-2-ylmethyl)methanesulfonamide

95%

Reagent Code: #230163
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CAS Number 1186049-30-8

science Other reagents with same CAS 1186049-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.22 g/mol
Formula C₆H₁₁F₃N₂O₂S
badge Registry Numbers
MDL Number MFCD11656044
thermostat Physical Properties
Melting Point 210°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonamide group enhances metabolic stability, while the trifluoromethyl group improves lipophilicity and bioavailability. Commonly employed in the development of selective enzyme inhibitors and receptor modulators due to its rigid structure and stereochemical purity. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿600.00
100mg
10-20 days ฿1,150.00
500mg
10-20 days ฿2,860.00
1g
10-20 days ฿4,360.00
5g
10-20 days ฿15,730.00
(R)-1,1,1-Trifluoro-N-(pyrrolidin-2-ylmethyl)methanesulfonamide
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonamide group enhances metabolic stability, while the trifluoromethyl group improves lipophilicity and bioavailability. Commonly employed in the development of selective enzyme inhibitors and receptor modulators due to its rigid structure and stereochemical purity. Also utilized in asymmetric synthesis to introduce chirality in drug candida

Used as a chiral building block in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its sulfonamide group enhances metabolic stability, while the trifluoromethyl group improves lipophilicity and bioavailability. Commonly employed in the development of selective enzyme inhibitors and receptor modulators due to its rigid structure and stereochemical purity. Also utilized in asymmetric synthesis to introduce chirality in drug candidates.

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