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AB44356

134-96-3 | Syringaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
5g 98% in stock $10.00 $7.00 -   +
25g 98% in stock $15.00 $10.00 -   +
100g 98% in stock $45.00 $31.00 -   +
500g 98% in stock $70.00 $49.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB44356
Chemical Name: Syringaldehyde
CAS Number: 134-96-3
Molecular Formula: C9H10O4
Molecular Weight: 182.1733
MDL Number: MFCD00006943
SMILES: COc1cc(C=O)cc(c1O)OC
NSC Number: 41153

 

Computed Properties
Complexity: 157  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • 4-Hydroxy-3,5-dimethoxybenzaldehyde, also known as $name$, is a versatile and important compound used in various chemical synthesis processes. In organic chemistry, this compound is utilized as a key building block for the synthesis of a wide range of organic molecules. With its unique structure and reactivity, 4-Hydroxy-3,5-dimethoxybenzaldehyde serves as a valuable substrate for the creation of complex chemical structures.One of the primary applications of 4-Hydroxy-3,5-dimethoxybenzaldehyde is in the preparation of pharmaceutical compounds. Chemists use this compound as a starting material to synthesize biologically active molecules, such as pharmaceutical drugs and natural product analogs. The presence of the hydroxy and methoxy groups in the molecule enhances its potential for forming specific chemical bonds that are crucial for drug development.Furthermore, 4-Hydroxy-3,5-dimethoxybenzaldehyde is widely employed in the synthesis of fragrances and flavoring agents. Its aromatic nature and functional groups make it a popular choice for creating unique scents and tastes in perfumes, cosmetics, and food products. By incorporating this compound into various chemical reactions, chemists can tailor the aroma and flavor profiles of a wide range of consumer products.In addition to its role in pharmaceuticals and fragrances, 4-Hydroxy-3,5-dimethoxybenzaldehyde is also used in materials science and polymer chemistry. It can be incorporated into polymer chains to impart specific properties such as UV resistance, antioxidant capabilities, and thermal stability. By integrating this compound into polymer matrices, researchers can tailor the performance of materials for various industrial applications.Overall, the versatile and multifaceted nature of 4-Hydroxy-3,5-dimethoxybenzaldehyde makes it an indispensable tool in chemical synthesis. Its diverse applications span across pharmaceuticals, fragrances, materials science, and beyond, showcasing its significance in the field of organic chemistry.
Literature
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