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Home  > Chemistry  > Heterocyclic Building Blocks  > Dioxolanes  > 2-Hydroxymethyl-1,3-dioxolane

AG74087

5694-68-8 | 2-Hydroxymethyl-1,3-dioxolane

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $15.00 $10.00 -   +
1g 97% in stock $29.00 $20.00 -   +
5g 97% in stock $90.00 $63.00 -   +
10g 97% in stock $150.00 $105.00 -   +
25g 97% in stock $320.00 $224.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AG74087
Chemical Name: 2-Hydroxymethyl-1,3-dioxolane
CAS Number: 5694-68-8
Molecular Formula: C4H8O3
Molecular Weight: 104.1045
MDL Number: MFCD08062572
SMILES: OCC1OCCO1
NSC Number: 163968

 

Computed Properties
Complexity: 48.9  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: -0.8  

 

 

Upstream Synthesis Route
  • The (1,3-Dioxolan-2-yl)methanol, also known as dioxolane alcohol, is a versatile chemical compound widely used in various chemical synthesis processes. Its unique structure provides several key applications in organic chemistry, making it a valuable reagent for chemical transformations.One of the primary uses of (1,3-Dioxolan-2-yl)methanol is as a protecting group for aldehydes and ketones. By forming a stable acetal linkage with the carbonyl group, this compound can mask reactive functionalities in molecules, allowing selective manipulations in complex organic synthesis sequences. This property is particularly useful in the construction of intricate molecular structures and the control of regioselectivity during transformations.Furthermore, (1,3-Dioxolan-2-yl)methanol can serve as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its compatibility with a wide range of reaction conditions and functional groups makes it a versatile tool for the preparation of diverse chemical entities. Additionally, the ease of deprotection of the dioxolane moiety ensures efficient access to the desired products without compromising yields or purities.In summary, the (1,3-Dioxolan-2-yl)methanol plays a crucial role in modern chemical synthesis, offering chemists a reliable means to control reactivity, selectivity, and functionality in complex molecular design. Its applications extend across multiple disciplines, showcasing its importance in advancing synthetic methodologies and enabling the creation of novel chemical entities.
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