2-(Pyridin-2-yloxy)propanoic acid

95%

Reagent Code: #227045
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CAS Number 168844-45-9

science Other reagents with same CAS 168844-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
badge Registry Numbers
MDL Number MFCD07364005
thermostat Physical Properties
Boiling Point 286.8±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.241±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of herbicides and anti-inflammatory agents. Its structure allows for selective interactions in biological systems, making it valuable in agrochemical research. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also serves as an intermediate in the preparation of pyridyloxy-based bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,600.00
inventory 100mg
10-20 days ฿7,800.00
inventory 250mg
10-20 days ฿13,000.00
inventory 1g
10-20 days ฿26,000.00

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2-(Pyridin-2-yloxy)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of herbicides and anti-inflammatory agents. Its structure allows for selective interactions in biological systems, making it valuable in agrochemical research. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also serves as an intermediate in the preparation of pyridyloxy-based bioactive molecules.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of herbicides and anti-inflammatory agents. Its structure allows for selective interactions in biological systems, making it valuable in agrochemical research. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also serves as an intermediate in the preparation of pyridyloxy-based bioactive molecules.

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