3-(Benzo[d][1,3]dioxol-5-yl)-2-cyanoacrylic acid

95%

Reagent Code: #141275
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CAS Number 51066-70-7

science Other reagents with same CAS 51066-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.17 g/mol
Formula C₁₁H₇NO₄
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MDL Number MFCD00759392
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of serotonin reuptake inhibitors and related central nervous system agents. Its structure supports conjugation and derivatization for use in medicinal chemistry, enabling the formation of cyanoacrylate derivatives with potential anti-inflammatory and neuroactive properties. Also employed in research settings for building complex heterocyclic systems due to its reactive cyano and carboxylic acid functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,130.00
inventory 250mg
10-20 days ฿13,810.00
inventory 1g
10-20 days ฿37,260.00
3-(Benzo[d][1,3]dioxol-5-yl)-2-cyanoacrylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of serotonin reuptake inhibitors and related central nervous system agents. Its structure supports conjugation and derivatization for use in medicinal chemistry, enabling the formation of cyanoacrylate derivatives with potential anti-inflammatory and neuroactive properties. Also employed in research settings for building complex heterocyclic systems due to its reactive cyano a

Used as a key intermediate in the synthesis of pharmaceuticals and biologically active compounds, particularly in the development of serotonin reuptake inhibitors and related central nervous system agents. Its structure supports conjugation and derivatization for use in medicinal chemistry, enabling the formation of cyanoacrylate derivatives with potential anti-inflammatory and neuroactive properties. Also employed in research settings for building complex heterocyclic systems due to its reactive cyano and carboxylic acid functional groups.

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