2-Amino-1-(butyldimethylsiloxy)butane

98%

Reagent Code: #88200
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CAS Number 811841-81-3

science Other reagents with same CAS 811841-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.40 g/mol
Formula C₁₀H₂₅NOSi
badge Registry Numbers
MDL Number MFCD03001670
inventory_2 Storage & Handling
Storage 2~8℃, dry, sealed

description Product Description

2-Amino-1-(butyldimethylsiloxy)butane is a specialty organic intermediate featuring a butyldimethylsilyl (BDS) protecting group on the primary alcohol moiety. This protection enables selective reactions at the free secondary amine group during multi-step organic syntheses, preventing unwanted side reactions from the hydroxyl functionality. It is particularly useful in the preparation of complex molecules for pharmaceuticals, agrochemicals, and natural product analogs, where precise control over functional group reactivity is required. Additionally, it serves as a building block for synthesizing silicon-functionalized compounds applied in advanced materials, such as specialty polymers and coatings with tailored properties. The protecting group can be readily removed under mild conditions post-reaction.

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Test Parameter Specification
Purity 97.5-100

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿999.00
inventory 1g
10-20 days ฿387.00
inventory 25g
10-20 days ฿3,438.00

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2-Amino-1-(butyldimethylsiloxy)butane
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2-Amino-1-(butyldimethylsiloxy)butane is a specialty organic intermediate featuring a butyldimethylsilyl (BDS) protecting group on the primary alcohol moiety. This protection enables selective reactions at the free secondary amine group during multi-step organic syntheses, preventing unwanted side reactions from the hydroxyl functionality. It is particularly useful in the preparation of complex molecules for pharmaceuticals, agrochemicals, and natural product analogs, where precise control over functiona

2-Amino-1-(butyldimethylsiloxy)butane is a specialty organic intermediate featuring a butyldimethylsilyl (BDS) protecting group on the primary alcohol moiety. This protection enables selective reactions at the free secondary amine group during multi-step organic syntheses, preventing unwanted side reactions from the hydroxyl functionality. It is particularly useful in the preparation of complex molecules for pharmaceuticals, agrochemicals, and natural product analogs, where precise control over functional group reactivity is required. Additionally, it serves as a building block for synthesizing silicon-functionalized compounds applied in advanced materials, such as specialty polymers and coatings with tailored properties. The protecting group can be readily removed under mild conditions post-reaction.

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