tert-Butyl 5-bromobenzo[d]thiazol-2-ylcarbamate

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Reagent Code: #168478
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CAS Number 1160573-06-7

science Other reagents with same CAS 1160573-06-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.21 g/mol
Formula C₁₂H₁₃BrN₂O₂S
badge Registry Numbers
MDL Number MFCD16036615
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. It plays a key role in the development of kinase inhibitors and other therapeutic agents due to the presence of the benzo[d]thiazole scaffold, which is known for its broad pharmacological properties. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites during multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting anti-inflammatory, anticancer, and antimicrobial agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,030.00
inventory 1g
10-20 days ฿18,100.00

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tert-Butyl 5-bromobenzo[d]thiazol-2-ylcarbamate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. It plays a key role in the development of kinase inhibitors and other therapeutic agents due to the presence of the benzo[d]thiazole scaffold, which is known for its broad pharmacological properties. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites during multi-step syntheses. Commonly employed in medicinal chemis

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. It plays a key role in the development of kinase inhibitors and other therapeutic agents due to the presence of the benzo[d]thiazole scaffold, which is known for its broad pharmacological properties. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites during multi-step syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting anti-inflammatory, anticancer, and antimicrobial agents.

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