tert-Butyl hex-5-ynoate

98%

Reagent Code: #149023
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CAS Number 73448-14-3

science Other reagents with same CAS 73448-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.24 g/mol
Formula C₁₀H₁₆O₂
badge Registry Numbers
MDL Number MFCD13192076
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its alkyne functionality allows for coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecules. The tert-butyl ester group offers stability during reactions and can be selectively deprotected under acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of bioactive compounds and functional materials.

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Test Parameter Specification
Appearance Yellow liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,690.00
inventory 250mg
10-20 days ฿3,400.00
inventory 1g
10-20 days ฿9,760.00
inventory 5g
10-20 days ฿35,260.00

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tert-Butyl hex-5-ynoate
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Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its alkyne functionality allows for coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecules. The tert-butyl ester group offers stability during reactions and can be selectively deprotected under acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of bioactive compounds and functional materials.

Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its alkyne functionality allows for coupling reactions, such as Sonogashira or click chemistry, enabling the construction of complex molecules. The tert-butyl ester group offers stability during reactions and can be selectively deprotected under acidic conditions, making it valuable in multi-step synthesis. Commonly employed in the development of bioactive compounds and functional materials.

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