4-Iodobut-1-ene

95%

Reagent Code: #200489
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CAS Number 7766-51-0

science Other reagents with same CAS 7766-51-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.00 g/mol
Formula C₄H₇I
badge Registry Numbers
MDL Number MFCD11848508
inventory_2 Storage & Handling
Storage -20°C, protected from light, dry, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules through its reactive alkene and iodide functionalities. The terminal double bond allows for addition reactions such as hydrohalogenation or epoxidation, while the iodine atom, as a good leaving group, enables formation of Grignard reagents or participation in coupling reactions like Suzuki, Heck, or Negishi couplings, making it valuable in pharmaceutical and agrochemical synthesis. It is also employed in the production of polymers and functionalized long-chain compounds due to its bifunctional nature. Its volatility and reactivity require careful handling in controlled environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿910.00
inventory 250mg
10-20 days ฿1,740.00
inventory 1g
10-20 days ฿4,740.00
inventory 5g
10-20 days ฿22,810.00
inventory 25g
10-20 days ฿91,210.00
4-Iodobut-1-ene
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules through its reactive alkene and iodide functionalities. The terminal double bond allows for addition reactions such as hydrohalogenation or epoxidation, while the iodine atom, as a good leaving group, enables formation of Grignard reagents or participation in coupling reactions like Suzuki, Heck, or Negishi couplings, making it valuable in pharmaceutical and agrochemical synthesis. It

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex molecules through its reactive alkene and iodide functionalities. The terminal double bond allows for addition reactions such as hydrohalogenation or epoxidation, while the iodine atom, as a good leaving group, enables formation of Grignard reagents or participation in coupling reactions like Suzuki, Heck, or Negishi couplings, making it valuable in pharmaceutical and agrochemical synthesis. It is also employed in the production of polymers and functionalized long-chain compounds due to its bifunctional nature. Its volatility and reactivity require careful handling in controlled environments.

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