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AA43313

127913-44-4 | (S)-4-Chloro-3-hydroxybutyronitrile

Packsize Purity Availability Price Discounted Price    Quantity
25g 98% in stock $14.00 $10.00 -   +
500g 98% in stock $236.00 $165.00 -   +
1kg 98% in stock $416.00 $292.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA43313
Chemical Name: (S)-4-Chloro-3-hydroxybutyronitrile
CAS Number: 127913-44-4
Molecular Formula: C4H6ClNO
Molecular Weight: 119.5495
MDL Number: MFCD00273363
SMILES: O[C@H](CCl)CC#N

 

Computed Properties
Complexity: 84.9  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: -0.1  

 

 

Upstream Synthesis Route
  • (S)-4-Chloro-3-hydroxybutyronitrile, also known as $name$, is a key intermediate in chemical synthesis with versatile applications. This compound plays a crucial role in organic chemistry as a building block for the synthesis of various important molecules. (S)-4-Chloro-3-hydroxybutyronitrile is commonly used in the pharmaceutical industry for the preparation of chiral pharmaceuticals, agrochemicals, and fine chemicals.One of the main applications of (S)-4-Chloro-3-hydroxybutyronitrile is in the synthesis of optically active compounds. Its chiral nature allows it to impart stereochemical control in reactions, leading to the formation of enantiopure products. This compound is particularly valuable in asymmetric synthesis, where the stereochemistry of the molecule plays a crucial role in determining its biological activity or properties.Additionally, (S)-4-Chloro-3-hydroxybutyronitrile can be used as a precursor for the preparation of various functionalized molecules, such as amino alcohols, amino acids, and heterocyclic compounds. Its reactive functional groups enable the introduction of diverse substituents, allowing for the synthesis of a wide range of complex organic compounds.Overall, (S)-4-Chloro-3-hydroxybutyronitrile serves as a valuable tool in chemical synthesis, offering chemists the opportunity to access structurally diverse and stereochemically pure molecules for applications in drug discovery, materials science, and other fields of research.
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