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Home  > (S)-1-(4-Methoxyphenyl)ethanamine

AB55792

41851-59-6 | (S)-1-(4-Methoxyphenyl)ethanamine

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $13.00 $9.00 -   +
5g 98% in stock $21.00 $15.00 -   +
10g 98% in stock $26.00 $19.00 -   +
25g 98% in stock $50.00 $35.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB55792
Chemical Name: (S)-1-(4-Methoxyphenyl)ethanamine
CAS Number: 41851-59-6
Molecular Formula: C9H13NO
Molecular Weight: 151.2056
MDL Number: MFCD00671660
SMILES: COc1ccc(cc1)[C@@H](N)C

 

Computed Properties
Complexity: 108  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • (S)-1-(4-Methoxyphenyl)ethanamine, also known as (S)-PMA, is a chiral compound that plays a crucial role in chemical synthesis. Asymmetric synthesis is a vital technique in modern organic chemistry for producing enantiomerically pure compounds, which are often required in pharmaceuticals, agrochemicals, and materials science. The use of (S)-PMA as a chiral building block enables the creation of optically pure molecules with specific biological activities or physical properties.One common application of (S)-1-(4-Methoxyphenyl)ethanamine in chemical synthesis is in the preparation of chiral amines and amino alcohols. By incorporating (S)-PMA as a starting material or a key intermediate, chemists can access enantiopure molecules that are essential for drug development, catalysis, and asymmetric synthesis. The use of (S)-PMA allows for the selective formation of one enantiomer over the other, leading to improved efficiency and selectivity in chemical reactions.Additionally, (S)-1-(4-Methoxyphenyl)ethanamine can serve as a valuable ligand in asymmetric catalysis. When coordinated to a metal center, (S)-PMA can activate substrates and facilitate enantioselective transformations, such as hydrogenation, C-C bond formation, and oxidation reactions. The unique steric and electronic properties of (S)-PMA make it a versatile tool for designing efficient and selective catalysts in organic synthesis.Overall, (S)-1-(4-Methoxyphenyl)ethanamine is a versatile and valuable compound in chemical synthesis, enabling the creation of complex molecules with high enantiomeric purity and tailored properties for various applications in the fields of pharmaceuticals, materials, and beyond.
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