Cas no 162515-67-5 (1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid)

1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid is a specialized organic compound featuring a disulfide bridge linking two cyclopropaneacetic acid moieties. This structure imparts unique reactivity, making it valuable in synthetic chemistry, particularly for crosslinking or functionalization applications. The cyclopropane rings contribute steric constraint and electronic effects, while the disulfide bond offers reversible redox properties, useful in dynamic covalent chemistry. Its bifunctional nature allows for selective modifications, enabling applications in polymer science, bioconjugation, and materials research. The compound's stability and controlled reactivity make it suitable for precise synthetic transformations, offering researchers a versatile tool for designing complex molecular architectures.
1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid structure
162515-67-5 structure
Product Name:1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid
CAS No:162515-67-5
MF:C12H18O4S2
MW:290.398921489716
CID:1060468
PubChem ID:9835654
Update Time:2025-11-02

1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid Chemical and Physical Properties

Names and Identifiers

    • 1,1'-[Dithiobis(methylene)]biscyclopropaneacetic Acid
    • CUVZSQALKWWFBI-UHFFFAOYSA-N
    • 2-{1-[({[1-(carboxymethyl)cyclopropyl]methyl}disulfanyl)methyl]cyclopropyl}acetic acid
    • 1,1'-[Dithiobis(methylene)]bis[cyclopropaneacetic acid]
    • 2-[1-[[[1-(Carboxymethyl)cyclopropyl]methyldisulfanyl]methyl]cyclopropyl]acetic acid
    • DB-259031
    • Cyclopropaneacetic acid, 1,1'-[dithiobis(methylene)]bis-
    • 162515-67-5
    • MM2JSU9FDG
    • 2,2'-((Disulfanediylbis(methylene))bis(cyclopropane-1,1-diyl))diacetic acid
    • SCHEMBL9069745
    • 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid
    • Inchi: 1S/C12H18O4S2/c13-9(14)5-11(1-2-11)7-17-18-8-12(3-4-12)6-10(15)16/h1-8H2,(H,13,14)(H,15,16)
    • InChI Key: CUVZSQALKWWFBI-UHFFFAOYSA-N
    • SMILES: S(CC1(CC(=O)O)CC1)SCC1(CC(=O)O)CC1

Computed Properties

  • Exact Mass: 290.06465140g/mol
  • Monoisotopic Mass: 290.06465140g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 9
  • Complexity: 314
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.1
  • Topological Polar Surface Area: 125?2

1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
D494160-50mg
1,1'-[Dithiobis(methylene)]biscyclopropaneacetic Acid
162515-67-5
50mg
$ 184.00 2023-09-07
TRC
D494160-500mg
1,1'-[Dithiobis(methylene)]biscyclopropaneacetic Acid
162515-67-5
500mg
$ 1455.00 2023-09-07

Additional information on 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid

Comprehensive Overview of 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid (CAS No. 162515-67-5)

1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid (CAS No. 162515-67-5) is a specialized organic compound with a unique molecular structure. This compound features a dithiobis(methylene) core linked to two cyclopropaneacetic acid moieties, making it a valuable intermediate in synthetic chemistry. Researchers and industries are increasingly interested in this compound due to its potential applications in pharmaceuticals, agrochemicals, and material science.

The chemical properties of 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid are influenced by its cyclopropane rings and carboxylic acid functional groups. These structural elements contribute to its reactivity, enabling it to participate in various chemical transformations. For instance, the dithiobis(methylene) group can act as a linker or a protective group in synthetic pathways, while the cyclopropaneacetic acid segments offer opportunities for further derivatization.

In recent years, the demand for 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid has grown, particularly in the pharmaceutical sector. Its unique structure makes it a candidate for drug discovery, especially in the development of small-molecule inhibitors and bioconjugates. Additionally, its potential use in agrochemical formulations has sparked interest among researchers exploring sustainable pest control solutions.

The synthesis of 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid typically involves multi-step organic reactions, including cyclopropanation and thioether formation. Advanced techniques such as microwave-assisted synthesis and catalysis have been employed to improve yield and efficiency. These innovations align with the broader trend of green chemistry, which emphasizes environmentally friendly synthetic methods.

From a commercial perspective, 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid is available through specialized chemical suppliers. Its pricing and availability may vary depending on purity and scale requirements. Companies involved in custom synthesis and contract research often seek this compound for niche applications, driving its market growth.

Safety and handling of 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid require standard laboratory precautions. While not classified as hazardous under typical conditions, proper storage in a cool, dry environment is recommended to maintain stability. Researchers should consult material safety data sheets (MSDS) for specific guidelines.

Looking ahead, the future of 1,1'-Dithiobis(methylene)biscyclopropaneacetic Acid appears promising, with ongoing studies exploring its utility in biomedical applications and advanced materials. As the scientific community continues to uncover its potential, this compound is likely to gain further attention in both academic and industrial settings.

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