3-Amino-3-(4-cyanophenyl)propanoic acid

95%

Reagent Code: #131612
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CAS Number 80971-95-5

science Other reagents with same CAS 80971-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.2 g/mol
Formula C₁₀H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD01871335
thermostat Physical Properties
Melting Point 226-228°(dec)
Boiling Point 395.4±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.28±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and enzyme inhibitors. Its structure supports the construction of complex organic compounds with potential activity in neurological and metabolic pathways. The presence of both amino and carboxylic acid functional groups allows for peptide-like coupling, making it valuable in medicinal chemistry for designing drug candidates. Also employed in the preparation of specialty polymers and functionalized materials where nitrile and amino groups can be further modified.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,160.00
inventory 250mg
10-20 days ฿8,760.00
inventory 1g
10-20 days ฿23,650.00

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3-Amino-3-(4-cyanophenyl)propanoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and enzyme inhibitors. Its structure supports the construction of complex organic compounds with potential activity in neurological and metabolic pathways. The presence of both amino and carboxylic acid functional groups allows for peptide-like coupling, making it valuable in medicinal chemistry for designing drug candidates. Also employed in the preparation of specialty polymers and functiona
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and enzyme inhibitors. Its structure supports the construction of complex organic compounds with potential activity in neurological and metabolic pathways. The presence of both amino and carboxylic acid functional groups allows for peptide-like coupling, making it valuable in medicinal chemistry for designing drug candidates. Also employed in the preparation of specialty polymers and functionalized materials where nitrile and amino groups can be further modified.
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