Iodomethyl methyl carbonate

92%

Reagent Code: #200724
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CAS Number 69862-08-4

science Other reagents with same CAS 69862-08-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.97 g/mol
Formula C₃H₅IO₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a versatile alkylating agent in organic synthesis, particularly for introducing (methoxycarbonyloxy)methyl groups. It is effective in the preparation of carbonates from alcohols and phenols under mild conditions. Commonly employed in the synthesis of pharmaceutical intermediates due to its selective reactivity and good leaving group properties. Also utilized in the development of prodrugs and protecting group strategies where controlled esterification is required. Its iodine moiety allows further functionalization via nucleophilic substitution or cross-coupling reactions, enhancing its utility in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,370.00
inventory 250mg
10-20 days ฿8,500.00
inventory 1g
10-20 days ฿14,040.00
inventory 5g
10-20 days ฿52,000.00
Iodomethyl methyl carbonate
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Used as a versatile alkylating agent in organic synthesis, particularly for introducing (methoxycarbonyloxy)methyl groups. It is effective in the preparation of carbonates from alcohols and phenols under mild conditions. Commonly employed in the synthesis of pharmaceutical intermediates due to its selective reactivity and good leaving group properties. Also utilized in the development of prodrugs and protecting group strategies where controlled esterification is required. Its iodine moiety allows further

Used as a versatile alkylating agent in organic synthesis, particularly for introducing (methoxycarbonyloxy)methyl groups. It is effective in the preparation of carbonates from alcohols and phenols under mild conditions. Commonly employed in the synthesis of pharmaceutical intermediates due to its selective reactivity and good leaving group properties. Also utilized in the development of prodrugs and protecting group strategies where controlled esterification is required. Its iodine moiety allows further functionalization via nucleophilic substitution or cross-coupling reactions, enhancing its utility in multi-step synthetic routes.

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