(R,Z)-4-((tert-Butyldimethylsilyl)oxy)-N,N-diphenylpent-2-enamide

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Reagent Code: #37793
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CAS Number 1820030-49-6

science Other reagents with same CAS 1820030-49-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 381.58 g/mol
Formula C₂₃H₃₁NO₂Si
badge Registry Numbers
MDL Number MFCD31381100
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a tert-butyldimethylsilyl (TBS) protecting group, makes it valuable in multi-step synthetic processes, particularly in the protection of hydroxyl groups during chemical reactions. The presence of the diphenylamide moiety enhances its stability and reactivity, allowing it to participate in various coupling reactions. It is often employed in the synthesis of pharmaceuticals and bioactive compounds, where selective protection and deprotection strategies are crucial. Additionally, the compound’s stereochemistry (R,Z) can be leveraged in asymmetric synthesis to achieve specific chiral targets, making it a useful tool in the development of enantiomerically pure substances.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,519.00
inventory 250mg
10-20 days ฿5,868.00
inventory 1g
10-20 days ฿17,613.00

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(R,Z)-4-((tert-Butyldimethylsilyl)oxy)-N,N-diphenylpent-2-enamide
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a tert-butyldimethylsilyl (TBS) protecting group, makes it valuable in multi-step synthetic processes, particularly in the protection of hydroxyl groups during chemical reactions. The presence of the diphenylamide moiety enhances its stability and reactivity, allowing it to participate in various coupling reactions. It is often employed in the synthesis of ph

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring a tert-butyldimethylsilyl (TBS) protecting group, makes it valuable in multi-step synthetic processes, particularly in the protection of hydroxyl groups during chemical reactions. The presence of the diphenylamide moiety enhances its stability and reactivity, allowing it to participate in various coupling reactions. It is often employed in the synthesis of pharmaceuticals and bioactive compounds, where selective protection and deprotection strategies are crucial. Additionally, the compound’s stereochemistry (R,Z) can be leveraged in asymmetric synthesis to achieve specific chiral targets, making it a useful tool in the development of enantiomerically pure substances.

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