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Home  > Chemistry  > Organic Building Blocks  > Phenols  > 3,5-Dihydroxybenzyl alcohol

AB38505

29654-55-5 | 3,5-Dihydroxybenzyl alcohol

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $9.00 $6.00 -   +
5g 95% in stock $22.00 $15.00 -   +
10g 95% in stock $42.00 $29.00 -   +
25g 97% in stock $92.00 $65.00 -   +
100g 97% in stock $357.00 $250.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB38505
Chemical Name: 3,5-Dihydroxybenzyl alcohol
CAS Number: 29654-55-5
Molecular Formula: C7H8O3
Molecular Weight: 140.1366
MDL Number: MFCD00016867
SMILES: OCc1cc(O)cc(c1)O

 

Computed Properties
Complexity: 95  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  
XLogP3: 0.3  

 

 

Upstream Synthesis Route
  • 5-(Hydroxymethyl)-1,3-benzenediol, also known as hydroxybenzyl alcohol, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the synthesis of various complex molecules. Its hydroxyl and benzyl functional groups make it a valuable intermediate in the production of pharmaceuticals, agrochemicals, and fine chemicals.One common application of 5-(Hydroxymethyl)-1,3-benzenediol is in the preparation of polymer resins and adhesives. The hydroxyl group allows for easy modification and incorporation into polymer chains, enhancing their adhesion and strength properties. Additionally, the benzyl group provides stability and compatibility with a wide range of substrates, making it a versatile component in the formulation of adhesives for various applications.Furthermore, in the field of organic synthesis, 5-(Hydroxymethyl)-1,3-benzenediol is utilized as a protecting group for alcohols and phenols. By selectively acylating the hydroxyl group with appropriate reagents, the compound can mask reactive functional groups, allowing for specific reactions to take place without unwanted side reactions. This strategy is commonly employed in the synthesis of complex natural products and pharmaceutical intermediates.Overall, the diverse applications of 5-(Hydroxymethyl)-1,3-benzenediol in chemical synthesis highlight its significance as a crucial building block in the creation of innovative materials and compounds across various industries.
Literature
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