D204803
Diphenylacetylene
98%
Sinônimo(s):
Tolan
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About This Item
Produtos recomendados
Nível de qualidade
Ensaio
98%
forma
crystals
pb
170 °C/19 mmHg (lit.)
pf
59-61 °C (lit.)
densidade
0.99 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
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
chave InChI
JRXXLCKWQFKACW-UHFFFAOYSA-N
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Categorias relacionadas
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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FRET detection of proteins using fluorescently doped electrospun nanofibers and pattern recognition.
Langmuir : the ACS journal of surfaces and colloids, 27(10), 6401-6408 (2011-04-16)
This paper reports the fabrication of solid-state nanofiber sensor arrays and their use for detection of multiple proteins using principal component analysis (PCA). Four cationic and anionic fluorescently embedded nanofibers are generated by an electrospinning method, yielding unique patterns of
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
Organic letters, 3(20), 3083-3086 (2001-09-28)
[reaction: see text] A variety of substituted beta- and gamma-carbolines have been prepared in good to excellent yields by the annulation of internal acetylenes by the tert-butylimines of N-substituted 3-iodoindole-2-carboxaldehydes and 2-haloindole-3-carboxaldehydes, respectively, in the presence of a palladium catalyst.
Angewandte Chemie (International ed. in English), 50(52), 12569-12571 (2011-12-17)
The conformational equilibrium of a pH-dependent switch based on an intramolecularly H-bonded diphenylacetylene can be predictably biased by using electron-donating or -withdrawing groups. Furthermore, protonation of the electron-donating dimethylamino group converts it into an electron-withdrawing dimethylammonium cation with a concomitant
The journal of physical chemistry. B, 114(45), 14657-14663 (2010-06-01)
DNA-mediated charge transfer has recently received a substantial attention because of its biological relevance in the DNA damage and DNA repair as well as the potential applications to nanoscale electronic devices. In contrast to the numerous mechanistic studies on oxidative
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