| Identification | More | [Name]
Tetraphenylmethane | [CAS]
630-76-2 | [Synonyms]
TETRAPHENYLMETHANE
1,1’,1’’,1’’’-methanetetrayltetrakisbenzene
1,1’,1’’,1’’’-methanethetrayltetrakis-benzen
Benzene, 1,1',1'',1'''-methanetetrayltetrakis-
benzene,1,1’,1’’,1’’’-methanetetrayltetrakis-
Methane, tetraphenyl-
methane,tetraphenyl-
tetraphenyl-methan
Tritylbenzene
Tetraphenylmethane,96%
Tri(phenyl)methylbenzene | [EINECS(EC#)]
211-144-0 | [Molecular Formula]
C25H20 | [MDL Number]
MFCD00014428 | [Molecular Weight]
320.43 | [MOL File]
630-76-2.mol |
| Chemical Properties | Back Directory | [Appearance]
white to pink powder or needles | [Melting point ]
281-286 °C
| [Boiling point ]
431 °C
| [density ]
1.0992 (estimate) | [refractive index ]
1.8430 (estimate) | [Fp ]
431°C | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
insoluble in Ether,Alcohol | [form ]
powder to crystal | [color ]
Light yellow to Brown | [Water Solubility ]
Insoluble in water. | [BRN ]
1913557 | [InChI]
InChI=1S/C25H20/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20H | [InChIKey]
PEQHIRFAKIASBK-UHFFFAOYSA-N | [SMILES]
C(C1=CC=CC=C1)(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1 | [CAS DataBase Reference]
630-76-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Tetraphenylmethane(630-76-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R40:Limited evidence of a carcinogenic effect. | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RTECS ]
PB4050000 | [HazardClass ]
IRRITANT | [HS Code ]
29029090 |
| Questions And Answer | Back Directory | [Background]
Molecules of tetrahedral symmetry, such as tetraphenylmethane (TPM) and its various analogues (sometimes quite distant) over the years, were amongst the most exploited models in crystal engineering. For example, phenyl embraces, which are cooperative supramolecular motifs composed by set of Csingle bondH ? π attractive interactions have been recognized as fundamental interactions responsible for dense crystal packing of tetrahedrally-shaped species such as tetraphenylphosphonium, tetraphenylarsonium, and tetraphenylborate compounds. Another example of the significant role of TPM-like molecules is the introduction and development of molecular tectonics. Molecular tectonics is a strategy for the predictable construction of crystalline arrays from molecules called tectons. An inextricable feature of any tecton molecule is its shape and binding abilities enforce specific and directional arrangements of the same or complementary molecules[1].
|
| Hazard Information | Back Directory | [Chemical Properties]
white to pink powder or needles | [Uses]
Tetraphenylmethane is used to prepare a tetrapyridone tecton, which forms a diamondoid network with large internal chambers. It is also used in the preparation of 1-{4-[tris-(4-acetyl-phenyl)-methyl]-phenyl}-ethanone by Friedel-Crafts acylation reaction with acetyl chloride using aluminum chloride as catalyst. | [References]
[1] Zar?ba, Jan K. “Tetraphenylmethane and tetraphenylsilane as building units of coordination polymers and supramolecular networks – A focus on tetraphosphonates.” Inorganic Chemistry Communications 86 (2017): Pages 172-186. |
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