N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thiomorpholine-4-carboxamide

95%

Reagent Code: #91012
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CAS Number 874298-05-2

science Other reagents with same CAS 874298-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.268 g/mol
Formula C₁₇H₂₅BN₂O₃S
badge Registry Numbers
MDL Number MFCD31716301
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic compounds, including potential drug candidates. The thiomorpholine moiety in its structure is often associated with pharmacological activity, particularly in the development of compounds targeting neurological disorders or infectious diseases. Researchers use this chemical to explore its potential in designing inhibitors for specific enzymes or receptors, contributing to the discovery of new therapeutic agents. Its application is also seen in the development of boron-containing drugs, which are gaining attention for their unique properties in drug delivery and targeting.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,582.00
inventory 50mg
10-20 days ฿14,382.00

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N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thiomorpholine-4-carboxamide
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic compounds, including potential drug candidates. The thiomorpholine moiety in its structure is often associated with pharmacological activity, particularly in the development of compounds targeting neurological disorde
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create complex organic compounds, including potential drug candidates. The thiomorpholine moiety in its structure is often associated with pharmacological activity, particularly in the development of compounds targeting neurological disorders or infectious diseases. Researchers use this chemical to explore its potential in designing inhibitors for specific enzymes or receptors, contributing to the discovery of new therapeutic agents. Its application is also seen in the development of boron-containing drugs, which are gaining attention for their unique properties in drug delivery and targeting.
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