(R)-4-(Iodomethyl)-2,2-dimethyl-1,3-dioxolane

≥95%

Reagent Code: #37673
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CAS Number 23735-39-9

science Other reagents with same CAS 23735-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.06 g/mol
Formula C₆H₁₁IO₂
badge Registry Numbers
MDL Number MFCD07367263
thermostat Physical Properties
Boiling Point 217.3°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.623g/cm3
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its iodine moiety makes it a versatile reagent for nucleophilic substitution reactions, enabling the introduction of the dioxolane ring into more complex molecular structures. This is particularly valuable in the synthesis of biologically active compounds, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing the selectivity and efficiency of chemical transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿57,789.00
inventory 250mg
10-20 days ฿23,121.00
inventory 100mg
10-20 days ฿13,212.00

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(R)-4-(Iodomethyl)-2,2-dimethyl-1,3-dioxolane
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This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its iodine moiety makes it a versatile reagent for nucleophilic substitution reactions, enabling the introduction of the dioxolane ring into more complex molecular structures. This is particularly valuable in the synthesis of biologically active compounds, where stereochemistry plays a critical role in efficacy

This compound is primarily utilized in organic synthesis as a chiral building block. It serves as a key intermediate in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. Its iodine moiety makes it a versatile reagent for nucleophilic substitution reactions, enabling the introduction of the dioxolane ring into more complex molecular structures. This is particularly valuable in the synthesis of biologically active compounds, where stereochemistry plays a critical role in efficacy. Additionally, it is employed in the development of chiral catalysts and ligands for asymmetric synthesis, enhancing the selectivity and efficiency of chemical transformations.

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