Description
4,7-Methano-1H-indenol, 3a,4,5,6,7,7a-hexahydro- (CAS No. 27137-33-3) is a high-purity organic compound with the molecular formula C10H14O. This bicyclic alcohol derivative is a versatile intermediate widely used in organic synthesis, pharmaceutical research, and specialty chemical manufacturing. Its unique structural framework makes it valuable for developing complex molecular architectures. The compound is supplied as a clear to pale-yellow liquid with a characteristic odor, ensuring consistent quality for laboratory and industrial applications. Available in various packaging options, including amber glass bottles and bulk containers, to suit your specific requirements.
Key Features:
- CAS Number: 27137-33-3
- Molecular Formula: C10H14O
- Synonyms: Hydroxy dicyclopentadiene, 3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-indenol
- Purity: ≥95% (GC)
- Appearance: Clear to pale-yellow liquid
- Storage: Store in a cool, dry place under inert atmosphere
Properties
- CAS Number: 27137-33-3
- Complexity: 209
- IUPAC Name: (1S,2R,7R)-tricyclo[5.2.1.02,6]dec-4-en-3-ol
- InChI: InChI=1S/C10H14O/c11-9-4-3-8-6-1-2-7(5-6)10(8)9/h3-4,6-11H,1-2,5H2/t6-,7+,8?,9?,10-/m1/s1
- InChI Key: HRWRJUVJOLBMST-DJAYFPKFSA-N
- Exact Mass: 150.104465066
- Molecular Formula: C10H14O
- Molecular Weight: 150.22
- SMILES: C1C[C@@H]2C[C@H]1[C@@H]3C2C=CC3O
- Topological: 20.2
- Monoisotopic Mass: 150.104465066
- Synonyms: 27137-33-3, Hydroxy dicyclopentadiene, EINECS 248-252-2, 3a,4,5,6,7,7a-Hexahydro-4,7-methano-1H-indenol, 4,7-Methano-1H-indenol, 3a,4,5,6,7,7a-hexahydro-, DTXSID50904362, DTXCID501333520, EINECS 253-436-0, 248-252-2, (4R,7S,7aR)-3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoinden-1-ol, HRWRJUVJOLBMST-DJAYFPKFSA-N, AKOS016010204
4,7-Methano-1H-indenol serves as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its rigid bicyclic structure makes it valuable for creating chiral building blocks in asymmetric synthesis. Researchers utilize this compound in developing novel catalysts and ligands for organic transformations. The alcohol functionality allows for further derivatization to produce esters, ethers, or other functionalized products.
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