(1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane | CAS No. 2825-82-3

(1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane

Basic Information

CAS Number

2825-82-3

Molecular Formula

C10H16

Molecular Weight

136.24 g/mol

AD

Basic Physical Properties

Boiling Point

185.55°C (rough estimate)

Flash Point

55°C

Refractive Index

1.4860 to 1.4900

C1CC2C3CCC(C3)C2C1

InChI

InChI=1S/C10H16/c1-2-9-7-4-5-8(6-7)10(9)3-1/h7-10H,1-6H2/t7-,8+,9+,10-

InChIKey

LPSXSORODABQKT-FIRGSJFUSA-N

LogP

2.832600000000001

Topological Polar Surface Area

0.0 Ų

Hydrogen Bond Donor/Acceptor

0 / 0

Complexity

134

Safety Information

View Safety Information

GHS Hazard Pictograms

H226H226

Hazard Statement

H226 Flammable liquid and vapor
Flammable liquids

Hazard Class

Class 3 Class 3

Synonyms & References

English

  • Q27253256
  • exo-3,4,8,9-Tetrahydrodicyclopentadiene
  • 4,7-Methano-1H-indene, octahydro-, (3a-alpha,4-beta,7-beta,7a-alpha)-
  • LPSXSORODABQKT-FIRGSJFUSA-N
  • (3aR,4S,7R,7aS)-rel-Octahydro-1H-4,7-methanoindene
  • exo-Trimethylenenorbornane
  • NCGC00260317-01
  • CS-0186059
  • JP-10
  • exo-Tetrahydrodicyclopentadiene
  • (1R,2S,6R,7S)-tricyclo[5.2.1.0?,?]decane
  • exo-Hexahydro-4,7-methanoindan
  • (3aalpha,4beta,7beta,7aalpha)-Octahydro-4,7-methano-1H-indene
  • DTXCID00809530
  • DTXSID2029244
  • exo-Tricyclo[5.2.1.02,6]decane
  • D92560
  • AKOS024462349
  • CAS-2825-82-3
  • JP-10 jet fuel
  • exo-Tetrahydrobicyclopentadiene
  • 2825-82-3
  • BS-22495
  • rel-(3aR,4S,7R,7aS)-Octahydro-4,7-methano-1H-indene
  • EINECS 220-585-8
  • (3a-trans,7a-trans)-octahydro-4r,7-methano-indene
  • 4,7-Methano-1H-indene, octahydro-, (3aR,4S,7R,7aS)-rel-
  • 1Z2JUO569N
  • (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane
  • octahydro-exo-4,7-methano-1h-indene
  • Tox21_202770

MDL Number

MFCD01714931

FAQ

What are the physical and chemical properties of (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane (CAS: 2825-82-3)?

(1R,2S,6R,7S)-Tricyclo[5.2.1.02,6]decane is a cyclic compound with a molecular weight of approximately 218.36 g/mol. It is a colorless, crystalline solid with a melting point of 44-46°C. This compound has limited water solubility, and it is more soluble in organic solvents such as ethanol and acetone. It is relatively stable under normal conditions but can react with strong acids and bases. It's important to handle it under appropriate safety protocols to minimize risk.

How is (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane (CAS: 2825-82-3) typically synthesized?

(1R,2S,6R,7S)-Tricyclo[5.2.1.02,6]decane can be synthesized via a ring-opening polymerization of cyclohexene oxide followed by a cyclization step. This process typically uses a Lewis acid as a catalyst, such as BF3, to promote the polymerization. The selectivity and yield of the reaction can be influenced by the choice of catalyst and reaction conditions, such as temperature and solvent selection. Proper handling of the catalyst and reaction mixture is essential to ensure safety and yield.

What industries use (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane (CAS: 2825-82-3)?

(1R,2S,6R,7S)-Tricyclo[5.2.1.02,6]decane is used in various industries, including pharmaceuticals for the synthesis of chiral intermediates, polymers for the production of specialty chemicals, and as a sensor material in certain applications. It is also used in the development of semiconductors due to its unique structure and properties. Its specific use cases often depend on the quality and purity of the compound.

What precautions should be taken when handling (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane (CAS: 2825-82-3)?

When handling (1R,2S,6R,7S)-tricyclo[5.2.1.02,6]decane, it is crucial to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat to avoid skin contact and eye irritation. The compound should be stored in a cool, dry place away from strong acids and bases. In case of a spill, it should be cleaned up carefully using appropriate safety measures, and the site should be decontaminated. Always refer to the Safety Data Sheet (SDS) for detailed handling information and emergency procedures.

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