4-(3-Bromo-benzenesulfonyl)-piperazine-1-carboxylicacidtert-butylester

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Reagent Code: #152162
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CAS Number 937014-80-7

science Other reagents with same CAS 937014-80-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.307 g/mol
Formula C₁₅H₂₁BrN₂O₄S
badge Registry Numbers
MDL Number MFCD12024910
thermostat Physical Properties
Boiling Point 495.2±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.451±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It plays a key role in the development of kinase inhibitors and other targeted therapies due to the presence of reactive functional groups that allow for further chemical modifications. The tert-butyl ester group protects the carboxylic acid during synthesis, enabling selective deprotection and coupling in multi-step reactions. Its sulfonyl and piperazine moieties are commonly found in drug candidates targeting neurological disorders, inflammation, and cancer. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,620.00
inventory 5g
10-20 days ฿7,070.00
inventory 25g
10-20 days ฿30,690.00

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4-(3-Bromo-benzenesulfonyl)-piperazine-1-carboxylicacidtert-butylester
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It plays a key role in the development of kinase inhibitors and other targeted therapies due to the presence of reactive functional groups that allow for further chemical modifications. The tert-butyl ester group protects the carboxylic acid during synthesis, enabling selective deprotection and coupling in multi-step reactions. Its sulfonyl and piperazine moieties are commonly found in drug

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. It plays a key role in the development of kinase inhibitors and other targeted therapies due to the presence of reactive functional groups that allow for further chemical modifications. The tert-butyl ester group protects the carboxylic acid during synthesis, enabling selective deprotection and coupling in multi-step reactions. Its sulfonyl and piperazine moieties are commonly found in drug candidates targeting neurological disorders, inflammation, and cancer. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies.

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