| Identification | Back Directory | [Name]
TRIPTYCENE | [CAS]
477-75-8 | [Synonyms]
TRIPTYCENE
Tryptycene
RCL S60268
Triptycene,99%
TRIPTYCENE 99%
Triptycene,98+%
S-1,2-pentadiol
RARECHEM AQ BC 8A30
9-Hydroxytriptycene
Tribenzobicyclo[2.2.2]octatriene
9,10-Dihydro-9,10-o-benzenoanthracene
9,10-O-BENZENO-9,10-DIHYDROANTHRACENE
9,10-o-Benzenoanthracene, 9,10-dihydro-
Anthracene, 9,10-dihydro-9,10-O-benzeno-
9,10-[1,2]Benzeno-9,10-dihydroanthracene
9,10-Dihydro-9,10-[1,2]benzenoanthracene
9,10[1',2']-Benzenoanthracene,9,10-dihydro-
Triptycene9,10-o-Benzeno-9,10-dihydroanthracene | [EINECS(EC#)]
207-519-3 | [Molecular Formula]
C20H14 | [MDL Number]
MFCD00003813 | [MOL File]
477-75-8.mol | [Molecular Weight]
254.33 |
| Chemical Properties | Back Directory | [Appearance]
YELLOWISH-BEIGE TO GREYISH NEEDLE-LIKE CRYSTALS | [Melting point ]
252-254 °C(lit.)
| [Boiling point ]
332.54°C (rough estimate) | [density ]
1.1180 (estimate) | [refractive index ]
1.7040 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [Water Solubility ]
Insoluble in water | [form ]
powder to crystal | [color ]
White to Orange to Green | [Merck ]
14,9749 | [InChI]
InChI=1S/C20H14/c1-2-8-14-13(7-1)19-15-9-3-5-11-17(15)20(14)18-12-6-4-10-16(18)19/h1-12,19-20H | [InChIKey]
NGDCLPXRKSWRPY-UHFFFAOYSA-N | [SMILES]
C12C3C=CC=CC=3C(C3C=CC=CC1=3)C1C=CC=CC2=1 | [EPA Substance Registry System]
9,10[1',2']-Benzenoanthracene, 9,10-dihydro- (477-75-8) |
| Hazard Information | Back Directory | [Chemical Properties]
YELLOWISH-BEIGE TO GREYISH NEEDLE-LIKE CRYSTALS | [Uses]
Triptycene was used in determination of diffusion coefficients of radical ions of hexafluorobenzene, diphenylacetylene, triptycene and tetraphenylnapthalene in liquid n-hexane and n-hexadecane. | [Definition]
ChEBI: Triptycene is a member of anthracenes. | [General Description]
Triptycene is the structural building block for triptycene-based polymer of intrinsic microporosity due to its rigid, fused-ring skeleton and three-fold symmetry. Triptycene-based cylindrical macrotricyclic polyether containing two dibenzo[24]crown-8 cavities has been synthesized and proved to be a highly efficient host for the complexation with paraquat derivatives. | [Synthesis]
Triptycene can be prepared in one step in 28% yield from the Diels–Alder reaction of anthracene and benzyne. In this method, benzyne is generated by the reaction of magnesium and 2-bromofluorobenzene.
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
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400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
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021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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