4-Hydroxybut-2-ynoic acid

96%

Reagent Code: #196838
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CAS Number 7218-52-2

science Other reagents with same CAS 7218-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 100.07 g/mol
Formula C₄H₄O₃
badge Registry Numbers
MDL Number MFCD06658457
thermostat Physical Properties
Melting Point 115-116 °C
Boiling Point 319.2±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.429±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne, carboxylic acid, and hydroxy functional groups allow for versatile reactivity, including coupling reactions, cyclizations, and esterifications. It is particularly valuable in synthesizing butyrolactone derivatives and other heterocyclic compounds found in medicinal chemistry. Additionally, it serves as a building block in the development of specialty polymers and agrochemicals due to its rigid molecular structure and functional handles for further modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,700.00
inventory 250mg
10-20 days ฿6,170.00
inventory 1g
10-20 days ฿17,350.00
4-Hydroxybut-2-ynoic acid
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne, carboxylic acid, and hydroxy functional groups allow for versatile reactivity, including coupling reactions, cyclizations, and esterifications. It is particularly valuable in synthesizing butyrolactone derivatives and other heterocyclic compounds found in medicinal chemistry. Additionally, it serves as a building block in the developme

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne, carboxylic acid, and hydroxy functional groups allow for versatile reactivity, including coupling reactions, cyclizations, and esterifications. It is particularly valuable in synthesizing butyrolactone derivatives and other heterocyclic compounds found in medicinal chemistry. Additionally, it serves as a building block in the development of specialty polymers and agrochemicals due to its rigid molecular structure and functional handles for further modification.

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