2-(4-Chlorobutyl)-1,3-dioxolane

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Reagent Code: #160767
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CAS Number 118336-86-0

science Other reagents with same CAS 118336-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.63 g/mol
Formula C₇H₁₃ClO₂
badge Registry Numbers
MDL Number MFCD00043136
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its functional groups allow for ring-opening reactions and alkylation processes, making it valuable in constructing complex molecules. It is particularly useful in the development of active pharmaceutical ingredients where a chlorobutyl spacer with protected carbonyl functionality is needed. Additionally, it can act as a building block in the synthesis of heterocyclic compounds and specialty polymers. Due to the reactivity of the chloride and the acetal group, it enables selective transformations under controlled conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿650.00
inventory 5g
10-20 days ฿2,950.00
inventory 10g
10-20 days ฿5,850.00
inventory 25g
10-20 days ฿14,590.00
inventory 100g
10-20 days ฿58,250.00

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2-(4-Chlorobutyl)-1,3-dioxolane
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its functional groups allow for ring-opening reactions and alkylation processes, making it valuable in constructing complex molecules. It is particularly useful in the development of active pharmaceutical ingredients where a chlorobutyl spacer with protected carbonyl functionality is needed. Additionally, it can act as a building block in the synthesis of heterocyclic com

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its functional groups allow for ring-opening reactions and alkylation processes, making it valuable in constructing complex molecules. It is particularly useful in the development of active pharmaceutical ingredients where a chlorobutyl spacer with protected carbonyl functionality is needed. Additionally, it can act as a building block in the synthesis of heterocyclic compounds and specialty polymers. Due to the reactivity of the chloride and the acetal group, it enables selective transformations under controlled conditions.

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