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Home  > (S)-(-)-3-Cyclohexenecarboxylic acid

AB50962

5708-19-0 | (S)-(-)-3-Cyclohexenecarboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $6.00 $4.00 -   +
5g 98% in stock $10.00 $7.00 -   +
10g 98% in stock $12.00 $8.00 -   +
25g 98% in stock $15.00 $10.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB50962
Chemical Name: (S)-(-)-3-Cyclohexenecarboxylic acid
CAS Number: 5708-19-0
Molecular Formula: C7H10O2
Molecular Weight: 126.1531
MDL Number: MFCD08275437
SMILES: OC(=O)[C@H]1CCC=CC1

 

Computed Properties
Complexity: 138  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • (S)-(-)-3-Cyclohexenecarboxylic acid is a valuable compound widely used in chemical synthesis for its versatile applications. Its primary function lies in its ability to act as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its specific stereochemistry, (S)-(-)-3-Cyclohexenecarboxylic acid plays a crucial role in the asymmetric synthesis of complex molecules.This compound is often employed in the creation of chiral ligands, catalysts, and intermediates that are essential for the production of enantiopure compounds. Its unique structure allows for selective reactions, leading to the formation of molecules with high optical purity. In addition, (S)-(-)-3-Cyclohexenecarboxylic acid is utilized in the preparation of specialized materials such as polymers and advanced materials with tailored properties.Furthermore, this compound serves as a key component in the development of new synthetic methodologies and strategies in organic chemistry. Its involvement in various chemical transformations enables chemists to access diverse structural motifs and functional groups efficiently. Overall, the application of (S)-(-)-3-Cyclohexenecarboxylic acid in chemical synthesis significantly contributes to advancing the field of organic chemistry and broadening the scope of accessible molecules.
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