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AB40272

305-01-1 | Esculetin

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $3.00 $2.00 -   +
250mg 98% in stock $6.00 $4.00 -   +
5g 98% in stock $24.00 $17.00 -   +
10g 98% in stock $42.00 $30.00 -   +
25g 98% in stock $104.00 $73.00 -   +
100g 98% in stock $360.00 $252.00 -   +

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*All prices are in USD.

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Description
Catalog Number: AB40272
Chemical Name: Esculetin
CAS Number: 305-01-1
Molecular Formula: C9H6O4
Molecular Weight: 178.14153999999994
MDL Number: MFCD00006874
SMILES: O=c1ccc2c(o1)cc(c(c2)O)O
NSC Number: 26428

 

Computed Properties
Complexity: 248  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
XLogP3: 1.2  

 

 

Upstream Synthesis Route 
  • 6,7-Dihydroxy-2H-chromen-2-one, also known as esculetin, is a versatile compound widely used in chemical synthesis. As a natural coumarin derivative, it serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and organic materials.In chemical synthesis, esculetin plays a crucial role as a starting material for the production of diverse compounds. Its hydroxyl groups enable facile functionalization through various chemical reactions, such as esterification, etherification, and oxidation. This reactivity allows for the modification of esculetin to tailor its properties for specific applications.One common application of 6,7-Dihydroxy-2H-chromen-2-one in chemical synthesis is in the synthesis of novel anticoagulant drugs. By derivatizing esculetin with specific functional groups, chemists can design molecules with enhanced anticoagulant properties, providing potential treatments for thrombotic disorders.Additionally, esculetin's structural features make it a valuable intermediate in the development of natural product-inspired compounds with promising biological activities. Its presence in various medicinal plants has sparked interest in exploring its potential as a lead compound for drug discovery efforts.Overall, the adaptability and reactivity of 6,7-Dihydroxy-2H-chromen-2-one make it a valuable tool in chemical synthesis for creating diverse compounds with applications in pharmaceuticals, agrochemicals, and other industries.
Literature
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