3-Iodobut-2-enoic acid
95%
Reagent
Code: #200630
CAS Number
89033-14-7
blur_circular Chemical Specifications
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Molecular Information
Weight
211.99 g/mol
Formula
C₄H₅IO₂
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Registry Numbers
MDL Number
MFCD29059389
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Physical Properties
Melting Point
108-108.5 °C
Boiling Point
250.7±23.0 °C(Predicted)
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Storage & Handling
Density
2.090±0.06 g/cm3(Predicted)
Storage
2-8°C
description Product Description
Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective transformations due to the presence of both iodine and carboxylic acid functional groups. Commonly employed in coupling reactions, such as Suzuki or Heck reactions, where the iodine moiety acts as a reactive site for carbon-carbon bond formation. Also utilized in the synthesis of bioactive molecules, including antimicrobial and anti-inflammatory agents. The alpha,beta-unsaturated system enables conjugate addition reactions, expanding its utility in building complex organic frameworks.
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