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AI49184

37493-16-6 | (S)-1-Chloro-2-propanol

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $63.00 $45.00 -   +
1g 97% in stock $145.00 $102.00 -   +
5g 97% in stock $491.00 $344.00 -   +
10g 97% in stock $945.00 $661.00 -   +
25g 97% in stock $1,844.00 $1,291.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI49184
Chemical Name: (S)-1-Chloro-2-propanol
CAS Number: 37493-16-6
Molecular Formula: C3H7ClO
Molecular Weight: 94.5401
MDL Number: MFCD01862133
SMILES: C[C@@H](CCl)O

 

Computed Properties
Complexity: 22.9  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 5  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 0.6  

 

 

Upstream Synthesis Route
  • (S)-1-Chloropropan-2-ol, also known as (S)-Hydroxy-1-chloropropane, is a valuable compound widely used in chemical synthesis. Its chirality and unique structure make it a versatile building block in organic chemistry.One of the key applications of (S)-1-Chloropropan-2-ol is in the synthesis of pharmaceuticals and agrochemicals. Its chiral nature allows for the creation of enantiopure compounds, which are important in drug development to ensure efficacy and reduce potential side effects.Furthermore, (S)-1-Chloropropan-2-ol can be used in the preparation of chiral ligands for asymmetric catalysis. These ligands play a crucial role in controlling the stereochemistry of chemical reactions, enabling the production of complex molecules with high enantioselectivity.Additionally, this compound serves as a starting material for the synthesis of various fine chemicals, such as flavors, fragrances, and advanced materials. Its ability to undergo various chemical transformations, including nucleophilic substitution and oxidation reactions, makes it a valuable precursor in organic synthesis.Overall, (S)-1-Chloropropan-2-ol is a versatile compound with broad applications in chemical synthesis, particularly in the fields of pharmaceuticals, agrochemicals, and asymmetric catalysis. Its chiral properties and reactivity make it an essential building block for the creation of diverse and complex molecules with high enantioselectivity.
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