logo
Home  > (R)-(+)-1,2-Dithiolane-3-pentanoic acid

AA33577

1200-22-2 | (R)-(+)-1,2-Dithiolane-3-pentanoic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $8.00 $5.00 -   +
5g 95% in stock $23.00 $16.00 -   +
10g 95% in stock $32.00 $22.00 -   +
25g 95% in stock $49.00 $34.00 -   +
100g 95% in stock $129.00 $90.00 -   +
500g 95% in stock $471.00 $330.00 -   +

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

*All prices are in USD.

Request Bulk Quote
Description
Catalog Number: AA33577
Chemical Name: (R)-(+)-1,2-Dithiolane-3-pentanoic acid
CAS Number: 1200-22-2
Molecular Formula: C8H14O2S2
Molecular Weight: 206.3256
MDL Number: MFCD01631142
SMILES: OC(=O)CCCC[C@H]1SSCC1

 

Computed Properties
Complexity: 150  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 5  
XLogP3: 1.7  

 

 

Upstream Synthesis Route 
  • (R)-(+)-1,2-Dithiolane-3-pentanoic acid, commonly known as $name$, is a versatile compound widely used in chemical synthesis. This chiral building block plays a crucial role in asymmetric synthesis, where the chirality of the molecule is essential for the desired optical properties of the final product.In chemical synthesis, (R)-(+)-1,2-Dithiolane-3-pentanoic acid serves as a key precursor in the creation of various complex organic molecules. Its unique structure allows for selective reactions with other compounds, leading to the formation of new carbon-carbon or carbon-heteroatom bonds with high stereochemical control. This makes it particularly valuable in the development of pharmaceuticals, agrochemicals, and fine chemicals where precise control over stereochemistry is crucial for the efficacy and safety of the end products.Additionally, (R)-(+)-1,2-Dithiolane-3-pentanoic acid has found applications in the synthesis of natural products, where its chirality can mimic the stereochemistry found in nature. By incorporating this compound into synthetic pathways, chemists can access a wide range of natural product analogs with potentially enhanced biological activities.Overall, the versatility and utility of (R)-(+)-1,2-Dithiolane-3-pentanoic acid in chemical synthesis make it a valuable tool for creating complex molecules with specific stereochemical properties, paving the way for the development of novel drugs, materials, and other functional compounds.
Literature
FEATURED PRODUCTS