11-Cyano-1-undecanoicacid

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Reagent Code: #164450
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CAS Number 5810-18-4

science Other reagents with same CAS 5810-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.30 g/mol
Formula C₁₂H₂₁NO₂
badge Registry Numbers
MDL Number MFCD00002731
thermostat Physical Properties
Melting Point 57 °C
Boiling Point 381.7±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.984±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, allows for dual functional reactivity, enabling the formation of amides, esters, and other derivatives. Commonly employed in the development of specialty polymers and as a building block in the synthesis of nitrile-containing compounds with biological activity. Also utilized in research settings for modifying molecular frameworks in medicinal chemistry projects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,190.00
inventory 250mg
10-20 days ฿13,170.00
inventory 1g
10-20 days ฿41,330.00

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11-Cyano-1-undecanoicacid
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, allows for dual functional reactivity, enabling the formation of amides, esters, and other derivatives. Commonly employed in the development of specialty polymers and as a building block in the synthesis of nitrile-containing compounds with biological activity. Also utilized in research settings for modifying molecul

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, allows for dual functional reactivity, enabling the formation of amides, esters, and other derivatives. Commonly employed in the development of specialty polymers and as a building block in the synthesis of nitrile-containing compounds with biological activity. Also utilized in research settings for modifying molecular frameworks in medicinal chemistry projects.

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