2-Hexyl-4-pentynoic Acid

95%(T)

Reagent Code: #195162
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CAS Number 96017-59-3

science Other reagents with same CAS 96017-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.26 g/mol
Formula C₁₁H₁₈O₂
badge Registry Numbers
MDL Number MFCD00946863
inventory_2 Storage & Handling
Density 0.9399999999999999
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as a building block in organic synthesis, this compound serves in the preparation of specialty esters for fragrance and flavor applications due to its unique fatty-acid-like structure with alkyne functionality. Its terminal alkyne group allows for use in click chemistry reactions, particularly in pharmaceutical research for constructing complex molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Additionally, it finds use in polymer chemistry as a monomer or modifier to introduce reactive sites into polymeric chains, enabling cross-linking or functionalization. The compound’s long alkyl chain also imparts lipophilic character, making it suitable for designing bioactive molecules with improved membrane permeability.

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inventory 5g
10-20 days ฿10,710.00

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2-Hexyl-4-pentynoic Acid
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Used primarily as a building block in organic synthesis, this compound serves in the preparation of specialty esters for fragrance and flavor applications due to its unique fatty-acid-like structure with alkyne functionality. Its terminal alkyne group allows for use in click chemistry reactions, particularly in pharmaceutical research for constructing complex molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Additionally, it finds use in polymer chemistry as a monomer or modifier to intr

Used primarily as a building block in organic synthesis, this compound serves in the preparation of specialty esters for fragrance and flavor applications due to its unique fatty-acid-like structure with alkyne functionality. Its terminal alkyne group allows for use in click chemistry reactions, particularly in pharmaceutical research for constructing complex molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC). Additionally, it finds use in polymer chemistry as a monomer or modifier to introduce reactive sites into polymeric chains, enabling cross-linking or functionalization. The compound’s long alkyl chain also imparts lipophilic character, making it suitable for designing bioactive molecules with improved membrane permeability.

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