5-iodo-1-pentanol acetate

98%

Reagent Code: #200788
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CAS Number 65921-65-5

science Other reagents with same CAS 65921-65-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.08 g/mol
Formula C₇H₁₃IO₂
badge Registry Numbers
MDL Number MFCD25965901
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of radiolabeled compounds for medical imaging and pharmaceutical research. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in the development of tracers for studying biological pathways. Also employed in the synthesis of specialty polymers and functionalized molecules where a protected alcohol with a terminal halogen is required. The acetate group offers stability during reactions and can be selectively deprotected to release the alcohol for further derivatization.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,420.00
inventory 25g
10-20 days ฿4,960.00
inventory 100g
10-20 days ฿14,870.00
5-iodo-1-pentanol acetate
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Used as an intermediate in organic synthesis, particularly in the preparation of radiolabeled compounds for medical imaging and pharmaceutical research. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in the development of tracers for studying biological pathways. Also employed in the synthesis of specialty polymers and functionalized molecules where a protected alcohol with a terminal halogen is required. The acetate group offers stability during reacti

Used as an intermediate in organic synthesis, particularly in the preparation of radiolabeled compounds for medical imaging and pharmaceutical research. Its iodine functionality allows for easy incorporation of radioactive isotopes, making it valuable in the development of tracers for studying biological pathways. Also employed in the synthesis of specialty polymers and functionalized molecules where a protected alcohol with a terminal halogen is required. The acetate group offers stability during reactions and can be selectively deprotected to release the alcohol for further derivatization.

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