Tert-butyl 4-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetyl)piperazine-1-carboxylate

95%

Reagent Code: #36323
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CAS Number 1401697-54-8

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blur_circular Chemical Specifications

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Weight 446.3448 g/mol
Formula C₂₃H₃₅BN₂O₆
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily used in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those involving piperazine and boronic ester functionalities. The boronic ester group is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl-protected piperazine moiety is often utilized to enhance the stability and solubility of compounds during synthetic processes, making it a versatile building block in the design of drug candidates targeting various diseases. Its applications extend to the development of potential therapeutics for cancer, neurological disorders, and infectious diseases.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿88,722.00
inventory 250mg
10-20 days ฿12,222.00
inventory 1g
10-20 days ฿29,592.00

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Tert-butyl 4-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetyl)piperazine-1-carboxylate
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This chemical is primarily used in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those involving piperazine and boronic ester functionalities. The boronic ester group is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionall

This chemical is primarily used in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those involving piperazine and boronic ester functionalities. The boronic ester group is valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl-protected piperazine moiety is often utilized to enhance the stability and solubility of compounds during synthetic processes, making it a versatile building block in the design of drug candidates targeting various diseases. Its applications extend to the development of potential therapeutics for cancer, neurological disorders, and infectious diseases.

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