CAS 933-60-8

4,7-Methano-1H-indene,3a,4,7,7a-tetrahydro-, (3aR,4R,7S,7aS)-rel-

Description:

4,7-Methano-1H-indene, 3a,4,7,7a-tetrahydro-, (3aR,4R,7S,7aS)-rel- is a bicyclic organic compound characterized by its unique structure that includes a fused indene and cyclopentane framework. This compound features a methano bridge, which contributes to its distinct stereochemistry and three-dimensional conformation. The stereochemical descriptors (3aR, 4R, 7S, 7aS) indicate specific spatial arrangements of its substituents, which can significantly influence its chemical reactivity and interactions. Typically, such compounds may exhibit interesting properties, including potential applications in organic synthesis or as intermediates in the production of more complex molecules. The presence of multiple chiral centers suggests that it may exist in various enantiomeric forms, which can have different biological activities. Additionally, the compound's stability, solubility, and reactivity can be influenced by factors such as temperature and solvent conditions. Overall, 4,7-Methano-1H-indene is a notable example of a complex organic structure with potential implications in various fields of chemistry and materials science.

Formula: C₁₀H₁₂

Synonyms:

• 4,7-Methano-1H-indene,3a,4,7,7a-tetrahydro-, (3aa,4b,7b,7aa)-
• 4,7-Methanoindene, 3a,4,7,7a-tetrahydro-, exo- (8CI)
• exo-Cyclopentadiene dimer
• exo-Dicyclopentadiene
• exo-Tricyclo[5.2.1.02,6]deca-3,8-diene

exo-Cyclopentadiene Dimer (80% Purity)

Controlled Product

CAS: 933-60-8

Applications exo-Cyclopentadiene dimer is used in surface-initiated poly(dicyclopentadiene) (pDCPD) films. These films were shown to provide effective barriers to the diffusion of aqueous ions in excess of 1 × 106 Ω·cm2.
References Deng, X., et al.: J. Phys. Chem. C, 122, 6033 (2018); Njoroge, I., et al.: Langmuir, 33, 13903 (2017);

Formula: C₁₀H₁₂

Purity: 80%

Color and Shape: Neat

Molecular weight: 132.202

Ref: TR-C995415