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AD65118

106797-69-7 | 3-(3-Phenoxyphenyl)propan-1-ol

Packsize Purity Availability Price Discounted Price    Quantity
1mg 2 weeks $105.00 $73.00 -   +
2mg 2 weeks $123.00 $86.00 -   +
3mg 2 weeks $149.00 $105.00 -   +
5mg 2 weeks $168.00 $118.00 -   +
10mg 2 weeks $193.00 $135.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD65118
Chemical Name: 3-(3-Phenoxyphenyl)propan-1-ol
CAS Number: 106797-69-7
Molecular Formula: C15H16O2
Molecular Weight: 228.2863
MDL Number: MFCD09028720
SMILES: OCCCc1cccc(c1)Oc1ccccc1

 

Computed Properties
Complexity: 199  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 5  
XLogP3: 3.3  

 

 

Upstream Synthesis Route
  • 3-(3-Phenoxyphenyl)propan-1-ol is a versatile compound commonly used in chemical synthesis due to its unique chemical properties and reactivity. This compound serves as a valuable building block in organic synthesis, specifically in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its distinct structural features, 3-(3-Phenoxyphenyl)propan-1-ol can participate in a range of important chemical transformations, such as acylation, alkylation, and oxidation reactions. Its functional groups enable it to serve as both a nucleophile and an electrophile in different synthetic pathways, allowing for the creation of complex molecular structures in a controlled and efficient manner.In organic synthesis, 3-(3-Phenoxyphenyl)propan-1-ol can be utilized to introduce the phenoxyphenyl moiety into target molecules, imparting specific biological or chemical properties. This compound's presence can enhance the pharmacological activity of drug candidates or confer desirable characteristics to agricultural compounds, making it a valuable tool in the development of new chemical entities.Furthermore, the reactivity of 3-(3-Phenoxyphenyl)propan-1-ol makes it a suitable candidate for the construction of chiral molecules, as it can be easily incorporated into asymmetric synthesis strategies to produce enantiomerically pure compounds. This compound's versatility and synthetic utility make it a valuable asset in the hands of chemists seeking to design novel materials and explore diverse chemical spaces.
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