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Key Documents

D204803

Sigma-Aldrich

Diphenylacetylene

98%

Synonym(s):

Tolan

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About This Item

Linear Formula:
C6H5C≡CC6H5
CAS Number:
Molecular Weight:
178.23
Beilstein:
606478
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

crystals

bp

170 °C/19 mmHg (lit.)

mp

59-61 °C (lit.)

density

0.99 g/mL at 25 °C (lit.)

SMILES string

c1ccc(cc1)C#Cc2ccccc2

InChI

1S/C14H10/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-10H

InChI key

JRXXLCKWQFKACW-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Anion-dependent switching: dynamically controlling the conformation of hydrogen-bonded diphenylacetylenes.
Ian M Jones et al.
Angewandte Chemie (International ed. in English), 50(20), 4597-4600 (2011-04-16)
Dai Nishimura et al.
The Journal of organic chemistry, 73(7), 2496-2502 (2008-03-14)
Novel [2]rotaxanes bearing alpha-cyclodextrin (alpha-CD) derivatives and a diphenylacetylene axis molecule with trinitrobenzene as a bulky stopper have been prepared to investigate the relative rotary movement of a ring relative to an axis molecule and that of an axis molecule
Guangyu Zhao et al.
Journal of the American Chemical Society, 128(41), 13575-13585 (2006-10-13)
Alpha-hydrogen abstraction and alpha-hydrogen migration reactions yield novel titanium(IV) complexes bearing terminal phosphinidene ligands. Via an alpha-H migration reaction, the phosphinidene ((tBu)nacnac)Ti=P[Trip](CH(2)(tBu) ((tBu)nacnac(-) = [Ar]NC((t)Bu)CHC((t)Bu)N[Ar], Ar = 2,6-(CHMe2)(2C6H3, Trip = 2,4,6-(i)Pr3C6H2) was prepared by the addition of the primary phosphide
Athanasia C Tzika et al.
Genome biology and evolution, 7(6), 1827-1841 (2015-07-03)
Despite the availability of deep-sequencing techniques, genomic and transcriptomic data remain unevenly distributed across phylogenetic groups. For example, reptiles are poorly represented in sequence databases, hindering functional evolutionary and developmental studies in these lineages substantially more diverse than mammals. In
Hiroaki Imoto et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(35), 8797-8803 (2018-05-03)
2,3,4,5-Tetraaryl-1-phenylarsoles were synthesized by utilizing safely generated diiodophenylarsine and zirconacyclopentadienes. The obtained peraryl arsoles showed aggregation-induced emission (AIE), where intense emission was observed in the solid states (quantum yields up to 0.61), whereas the corresponding solutions were very weakly emissive.

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