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AA11939

1137-42-4 | 4-Hydroxybenzophenone

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $15.00 $10.00 -   +
25g 98% in stock $16.00 $11.00 -   +
100g 98% in stock $30.00 $21.00 -   +
500g 98% in stock $95.00 $66.00 -   +

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Description
Catalog Number: AA11939
Chemical Name: 4-Hydroxybenzophenone
CAS Number: 1137-42-4
Molecular Formula: C13H10O2
Molecular Weight: 198.2173
MDL Number: MFCD00002355
SMILES: Oc1ccc(cc1)C(=O)c1ccccc1
NSC Number: 1887

 

Computed Properties
Complexity: 211  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 3.1  

 

 

Upstream Synthesis Route 
  • The (4-Hydroxyphenyl)(phenyl)methanone, also known as benzophenone phenylhydrazone, is a versatile compound widely utilized in the field of chemical synthesis. Its application in organic chemistry primarily revolves around its ability to act as a reagent in various transformations.One key application of (4-Hydroxyphenyl)(phenyl)methanone is its use in the synthesis of heterocyclic compounds. Through condensation reactions with suitable reagents, this compound can serve as a building block for the construction of diverse heterocycles with biological relevance.Additionally, (4-Hydroxyphenyl)(phenyl)methanone is commonly employed in the preparation of chiral ligands for asymmetric catalysis. Its presence can impart specific stereochemical properties to the resulting compounds, enabling the selective formation of desired enantiomers in chemical reactions.Furthermore, this compound finds utility in the development of new organic materials, such as dyes, polymers, and liquid crystals. Its structural features contribute to the design of functional materials with tailored properties for applications in optoelectronics and other advanced technologies.Overall, the (4-Hydroxyphenyl)(phenyl)methanone plays a fundamental role in the realm of chemical synthesis, offering a multitude of possibilities for creating novel compounds, elucidating reaction mechanisms, and advancing the frontiers of organic chemistry.
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