CAS 1568-80-5
:2,2′,3,3′-Tetrahydro-3,3,3′,3′-tetramethyl-1,1′-spirobi[1H-indene]-6,6′-diol
Description:
2,2′,3,3′-Tetrahydro-3,3,3′,3′-tetramethyl-1,1′-spirobi[1H-indene]-6,6′-diol, with CAS number 1568-80-5, is a chemical compound characterized by its complex spirobicyclic structure. This substance features multiple chiral centers, contributing to its stereochemical diversity. It is a colorless to pale yellow solid at room temperature and is typically insoluble in water but may dissolve in organic solvents. The presence of hydroxyl (-OH) groups in its structure indicates that it can participate in hydrogen bonding, which may influence its solubility and reactivity. This compound is of interest in organic synthesis and may exhibit biological activity, although specific applications and biological properties can vary. Its unique structure allows for potential use in various fields, including pharmaceuticals and materials science. As with many organic compounds, handling should be done with care, considering safety data and potential hazards associated with its use.
Formula:C21H24O2
InChI:InChI=1S/C21H24O2/c1-19(2)11-21(17-9-13(22)5-7-15(17)19)12-20(3,4)16-8-6-14(23)10-18(16)21/h5-10,22-23H,11-12H2,1-4H3
InChI key:InChIKey=SICLLPHPVFCNTJ-UHFFFAOYSA-N
SMILES:CC1(C)CC2(C=3C(C(C)(C)C2)=CC=C(O)C3)C=4C1=CC=C(O)C4
Synonyms:- 1,1′-Spirobi[1H-indene]-6,6′-diol, 2,2′,3,3′-tetrahydro-3,3,3′,3′-tetramethyl-
- 1,1′-Spirobi[indan]-6,6′-diol, 3,3,3′,3′-tetramethyl-
- 2,2',3,3'-Tetrahydro-3,3,3',3'-Tetramethyl-1,1'-Spirobi-1H-Indene- 6,6'-Diol
- 2,2′,3,3′-Tetrahydro-3,3,3′,3′-tetramethyl-1,1′-spirobi[1H-indene]-6,6′-diol
- 3,3,3',3'-Tetramethyl-2,2',3,3'-Tetrahydro-1,1'-Spirobi[Indene]-6,6'-Diol
- 3,3,3′,3′-Tetramethyl-1,1′-spirobi[indane]-6,6′-diol
- 3,3,3′,3′-Tetramethyl-1,1′-spirobiindan-6,6′-diol
- 3,3,3′,3′-Tetramethyl-1,1′-spirobisindan-6,6′-diol
- 3,3,3′,3′-Tetramethyl-1,1′-spirobisindane-6,6′-diol
- 3,3,3′,3′-Tetramethyl-1,1′-spiroindane-6,6′-diol
- 3,3,3′,3′-Tetramethyl-2,2′,3,3′-tetrahydro-1,1′-spirobi[indene]-6,6′-diol
- 3,3′-Spiro-bis(1,1-dimethyl-2,3-dihydro-1H-inden-5-ol)
- 6,6′-Dihydroxy-3,3,3′,3′-tetramethyl-1,1′-spirobiindane
- SI (diol)
- See more synonyms
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Found 7 products.
3,3,3',3'-Tetramethyl-2,2',3,3'-Tetrahydro-1,1'-Spirobi[Indene]-6,6'-Diol
CAS:3,3,3',3'-Tetramethyl-2,2',3,3'-Tetrahydro-1,1'-Spirobi[Indene]-6,6'-DiolPurity:98%Molecular weight:308.41g/mol3,3,3',3'-Tetramethyl-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-6,6'-diol
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:308.42098999023443,3,3',3'-Tetramethyl-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-6,6'-diol
CAS:Formula:C21H24O2Purity:>95.0%(HPLC)(qNMR)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:308.42HIV-1 integrase inhibitor 8
CAS:<p>HIV-1 integrase inhibitor 8 is an inhibitor of HIV-1 integrase. Integration is a required step in HIV replication [1].</p>Formula:C21H24O2Purity:98.91%Color and Shape:SolidMolecular weight:308.41Spirobiindane
CAS:<p>Spirobiindane is an aromatic hydrocarbon that has a hydroxyl group at the 3-position. It is used as a monomer in the fabrication of polycarbonates and coatings. Spirobiindane can be synthesized by Friedel-Crafts reaction with chloride or acid catalyst, followed by hydrogenation. The activation energy for this reaction is 11 kcal/mol. This product also has transport properties, which are important for its use in optoelectronics and polycarbonates.</p>Formula:C21H24O2Purity:Min. 95%Molecular weight:308.41 g/mol





