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AA00637

10004-17-8 | 1,3-DIOXOLANE-2-METHANOL, 2-METHYL-

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% 1 week $282.00 $197.00 -   +
250mg 95% 1 week $478.00 $335.00 -   +
1g 95% 1 week $1,288.00 $902.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA00637
Chemical Name: 1,3-DIOXOLANE-2-METHANOL, 2-METHYL-
CAS Number: 10004-17-8
Molecular Formula: C5H10O3
Molecular Weight: 118.1311
MDL Number: MFCD22071617
SMILES: OCC1(C)OCCO1

 

Upstream Synthesis Route
  • (2-Methyl-1,3-dioxolan-2-yl)methanol is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of various molecules and compounds. By acting as a precursor in diverse reactions, it enables the formation of complex structures with specific functionalities.One key application of (2-Methyl-1,3-dioxolan-2-yl)methanol is its use as a protecting group in organic synthesis. By selectively blocking certain functional groups within a molecule, this compound provides a means to control the reactivity of specific sites during a multi-step synthesis process. This protection-deprotection strategy is crucial for the successful creation of intricate molecular architectures.Furthermore, (2-Methyl-1,3-dioxolan-2-yl)methanol can participate in ring-opening reactions, yielding products with modified ring structures. This reactivity expands the synthetic possibilities, allowing for the introduction of new functional groups or the formation of diverse ring systems. Such transformations are essential for the design and construction of target molecules in medicinal chemistry, material science, and other research fields.Overall, the application of (2-Methyl-1,3-dioxolan-2-yl)methanol in chemical synthesis contributes significantly to the development of novel compounds with tailored properties and functionalities. Its versatility and reactivity make it a valuable tool for organic chemists aiming to explore new synthetic pathways and advance the frontiers of science.
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