tert-Butyl 7-bromoheptanoate

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Reagent Code: #149630
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CAS Number 51100-47-1

science Other reagents with same CAS 51100-47-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.19 g/mol
Formula C₁₁H₂₁O₂Br
badge Registry Numbers
MDL Number MFCD27924668
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its bromine functionality allows for further coupling reactions, such as palladium-catalyzed cross-couplings, enabling the construction of complex molecules. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, making it versatile for building blocks in synthetic pathways. Commonly employed in the preparation of functionalized heptanoic acid derivatives used in bioactive compound development.

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Test Parameter Specification
Appearance Light Yellow Liquid
Purity 96.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,440.00
inventory 250mg
10-20 days ฿1,920.00
inventory 1g
10-20 days ฿3,840.00
inventory 5g
10-20 days ฿12,800.00
inventory 10g
10-20 days ฿22,720.00
inventory 25g
10-20 days ฿51,200.00

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tert-Butyl 7-bromoheptanoate
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its bromine functionality allows for further coupling reactions, such as palladium-catalyzed cross-couplings, enabling the construction of complex molecules. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, making it versatile for building blocks in synthetic pathways. Commonly employed in the preparation of functionalized heptanoic acid derivatives used in bioac

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its bromine functionality allows for further coupling reactions, such as palladium-catalyzed cross-couplings, enabling the construction of complex molecules. The ester group can be hydrolyzed to yield carboxylic acids or reduced to alcohols, making it versatile for building blocks in synthetic pathways. Commonly employed in the preparation of functionalized heptanoic acid derivatives used in bioactive compound development.

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