logo
Home  > Chemistry  > Organic Building Blocks  > Phenols  > 1,8-Naphthalenediol

AB43208

569-42-6 | 1,8-Naphthalenediol

Packsize Purity Availability Price Discounted Price    Quantity
100mg >97% in stock $20.00 $14.00 -   +
250mg >97% in stock $23.00 $16.00 -   +
1g >97% in stock $32.00 $22.00 -   +
5g 95% in stock $57.00 $40.00 -   +
10g 95% in stock $90.00 $63.00 -   +
25g 95% in stock $195.00 $137.00 -   +
100g 95% in stock $700.00 $490.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB43208
Chemical Name: 1,8-Naphthalenediol
CAS Number: 569-42-6
Molecular Formula: C10H8O2
Molecular Weight: 160.1693
MDL Number: MFCD00042701
SMILES: Oc1cccc2c1c(O)ccc2

 

Computed Properties
Complexity: 142  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
XLogP3: 2.8  

 

 

Upstream Synthesis Route
  • Naphthalene-1,8-diol, also known as 1,8-dihydroxynaphthalene, is a key compound widely utilized in chemical synthesis for its versatile applications. This aromatic diol plays a crucial role in various organic reactions, primarily due to its ability to serve as a building block for the synthesis of a range of important compounds.In organic chemistry, Naphthalene-1,8-diol is often employed as a precursor for the synthesis of complex organic molecules, owing to its reactivity and structural features. One of the prominent applications of this compound is in the synthesis of dyes and pigments. By undergoing selective oxidation or functionalization reactions, Naphthalene-1,8-diol can be transformed into vibrant colorants used in industries such as textiles, cosmetics, and printing.Furthermore, Naphthalene-1,8-diol serves as a valuable intermediate in the production of pharmaceuticals and agrochemicals. Its versatile reactivity allows for the introduction of functional groups and structural modifications necessary for the development of bioactive compounds with desired properties. Additionally, the diol structure offers opportunities for the formation of chelating agents and coordination complexes used in catalysis and metal ion detection.Overall, Naphthalene-1,8-diol's significance in chemical synthesis lies in its role as a fundamental building block for the construction of diverse organic molecules with applications across multiple industries. Its reactivity, coupled with its unique structural properties, makes it a valuable tool for organic chemists seeking to design and synthesize novel compounds for various purposes.
Literature
FEATURED PRODUCTS