Allyl iodide

97%, copper stabilizer

Reagent Code: #134719
label
Alias Allyl iodide; 3-iodopropylene
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CAS Number 556-56-9

science Other reagents with same CAS 556-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.98 g/mol
Formula C₃H₅I
badge Registry Numbers
EC Number 209-130-4
MDL Number MFCD00001094
thermostat Physical Properties
Melting Point -99 °C
Boiling Point 102-103°C
inventory_2 Storage & Handling
Density 1.837 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as an alkylating agent in organic synthesis, particularly in the preparation of allylated compounds such as pharmaceuticals, agrochemicals, and fragrances. It serves as a source of the allyl group in reactions with nucleophiles due to its high reactivity. Employed in the synthesis of heterocyclic compounds and in palladium-catalyzed coupling reactions. Also utilized in the production of specialty monomers for polymers and in the modification of natural products to enhance biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿1,020.00
25g
10-20 days ฿2,490.00
100g
10-20 days ฿9,450.00
500g
10-20 days ฿46,780.00
2g
10-20 days ฿480.00
Allyl iodide
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Used as an alkylating agent in organic synthesis, particularly in the preparation of allylated compounds such as pharmaceuticals, agrochemicals, and fragrances. It serves as a source of the allyl group in reactions with nucleophiles due to its high reactivity. Employed in the synthesis of heterocyclic compounds and in palladium-catalyzed coupling reactions. Also utilized in the production of specialty monomers for polymers and in the modification of natural products to enhance biological activity.

Used as an alkylating agent in organic synthesis, particularly in the preparation of allylated compounds such as pharmaceuticals, agrochemicals, and fragrances. It serves as a source of the allyl group in reactions with nucleophiles due to its high reactivity. Employed in the synthesis of heterocyclic compounds and in palladium-catalyzed coupling reactions. Also utilized in the production of specialty monomers for polymers and in the modification of natural products to enhance biological activity.

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