4-(Iodomethyl)tetrahydro-2H-pyran

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Reagent Code: #199708
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CAS Number 101691-94-5

science Other reagents with same CAS 101691-94-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.06 g/mol
Formula C₆H₁₁IO
thermostat Physical Properties
Boiling Point 229.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its reactive iodomethyl group allows for efficient alkylation and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in the preparation of heterocyclic compounds and bioactive agents where a protected hydroxymethyl moiety is needed. The tetrahydro-2H-pyran ring acts as a protecting group for alcohols in multi-step synthesis, enabling selective transformations elsewhere in the molecule. Its stability under various reaction conditions and ease of deprotection make it ideal for use in peptide synthesis and drug development pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿174.00
inventory 1g
10-20 days ฿450.00

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4-(Iodomethyl)tetrahydro-2H-pyran
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Used primarily as a key intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its reactive iodomethyl group allows for efficient alkylation and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in the preparation of heterocyclic compounds and bioactive agents where a protected hydroxymethyl moiety is needed. The tetrahydro-2H-pyran ring acts as a protecting group for alcohols in multi-step synthesis, enabling selective trans

Used primarily as a key intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. Its reactive iodomethyl group allows for efficient alkylation and coupling reactions, making it valuable in constructing complex molecules. Commonly employed in the preparation of heterocyclic compounds and bioactive agents where a protected hydroxymethyl moiety is needed. The tetrahydro-2H-pyran ring acts as a protecting group for alcohols in multi-step synthesis, enabling selective transformations elsewhere in the molecule. Its stability under various reaction conditions and ease of deprotection make it ideal for use in peptide synthesis and drug development pathways.

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