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AG69000

620616-08-2 | (S)-2-Amino-2-(3-chlorophenyl)ethanol hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $33.00 $24.00 -   +
250mg 95% in stock $49.00 $35.00 -   +
1g 95% in stock $99.00 $70.00 -   +
5g 95% in stock $490.00 $343.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AG69000
Chemical Name: (S)-2-Amino-2-(3-chlorophenyl)ethanol hydrochloride
CAS Number: 620616-08-2
Molecular Formula: C8H11Cl2NO
Molecular Weight: 208.0850
MDL Number: MFCD12758101
SMILES: OC[C@H](c1cccc(c1)Cl)N.Cl

 

Computed Properties
Complexity: 121  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • (S)-2-Amino-2-(3-chlorophenyl)ethanol hydrochloride, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. Its primary application lies in the field of asymmetric synthesis, where it serves as a chiral building block for the preparation of various pharmaceuticals and fine chemicals.In organic chemistry, (S)-2-Amino-2-(3-chlorophenyl)ethanol hydrochloride is often employed as a key reagent in the synthesis of enantiomerically pure compounds. Its chiral nature imparts stereochemical control in reactions, enabling the selective formation of chiral centers with high enantiomeric excess. This makes it an essential tool for the production of optically pure drug molecules and other complex organic compounds.Moreover, the hydrochloride salt form of (S)-2-Amino-2-(3-chlorophenyl)ethanol offers the advantage of enhanced solubility and stability, facilitating its use in a wide range of chemical transformations. From the synthesis of pharmaceutical intermediates to the preparation of chiral ligands for catalysis, this compound finds diverse applications in the laboratory and industrial settings.Overall, (S)-2-Amino-2-(3-chlorophenyl)ethanol hydrochloride plays a crucial role in enabling the precise control of molecular chirality in chemical synthesis, making it an indispensable component in the toolkit of synthetic chemists.
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