Pyridine Hydroiodide

98%

Reagent Code: #225731
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CAS Number 18820-83-2

science Other reagents with same CAS 18820-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.01 g/mol
Formula C₅H₅N·HI
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a reagent in organic synthesis, particularly in the preparation of iodinated compounds. It serves as a source of hydriodic acid in situ when heated, facilitating reductions and cleavage reactions, such as the dealkylation of methyl esters or ethers. Commonly applied in the conversion of alcohols to alkyl iodides. Also utilized in the pharmaceutical industry for synthesizing active ingredients where controlled iodine release is required. Its role as a catalyst or additive in certain heterocyclic transformations enhances reaction efficiency under mild conditions.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,390.00
inventory 25g
10-20 days ฿37,800.00
Pyridine Hydroiodide
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Used as a reagent in organic synthesis, particularly in the preparation of iodinated compounds. It serves as a source of hydriodic acid in situ when heated, facilitating reductions and cleavage reactions, such as the dealkylation of methyl esters or ethers. Commonly applied in the conversion of alcohols to alkyl iodides. Also utilized in the pharmaceutical industry for synthesizing active ingredients where controlled iodine release is required. Its role as a catalyst or additive in certain heterocyclic t

Used as a reagent in organic synthesis, particularly in the preparation of iodinated compounds. It serves as a source of hydriodic acid in situ when heated, facilitating reductions and cleavage reactions, such as the dealkylation of methyl esters or ethers. Commonly applied in the conversion of alcohols to alkyl iodides. Also utilized in the pharmaceutical industry for synthesizing active ingredients where controlled iodine release is required. Its role as a catalyst or additive in certain heterocyclic transformations enhances reaction efficiency under mild conditions.

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