Name | Diphenylacetylene |
Synonyms | Tolan TOLAN DIPHENYLACETYLENE Diphenylacetylene 1,2-DIPHENYL ETHYNE 1,2-Diphenylacetylene (phenylethynyl)benzene (Phenylethynyl)benzene 1,2-Ethynediylbisbenzene Diphenyl acetylene (Tolan) 1,1'-ethyne-1,2-diyldibenzene 1,1'-(1,2-Ethanediyl)bisbenzene 1,1'-(1,2-Ethynediyl)bisbenzene 1,1'-(1,2-ethynediyl)bis-benzen |
CAS | 501-65-5 |
EINECS | 207-926-6 |
InChI | InChI=1/C12H10.C2H2/c1-3-7-11(8-4-1)12-9-5-2-6-10-12;1-2/h1-10H;1-2H |
InChIKey | JRXXLCKWQFKACW-UHFFFAOYSA-N |
Molecular Formula | C14H10 |
Molar Mass | 178.23 |
Density | 0.99 g/mL at 25 °C (lit.) |
Melting Point | 59-61 °C (lit.) |
Boling Point | 170 °C/19 mmHg (lit.) |
Flash Point | 170°C/19mm |
Water Solubility | Miscible with ether and hot alcohol. Immiscible with water. |
Appearance | Crystallization |
Specific Gravity | 0.99 |
Color | Light yellow to brownish |
Merck | 14,9504 |
BRN | 606478 |
Storage Condition | Sealed in dry,2-8°C |
Stability | Stable. Combustible. Incompatible with strong oxidizing agents. |
Refractive Index | 1.6415 (estimate) |
MDL | MFCD00004786 |
Physical and Chemical Properties | Colorless patchy crystals. Melting point 62.5 °c (60-61 °c), boiling point 300 °c, 170 °c (2.53kPa),90-97 °c (40Pa), relative density 0.966(100/4 °c). Soluble in hot ethanol and ether, insoluble in water. |
Use | for organic synthesis. |
Safety Description | S24/25 - Avoid contact with skin and eyes. S22 - Do not breathe dust. |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29029090 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Overview | The alkyne derivative diphenylacetylene occupies an important position in organic synthesis. Many natural products, drug molecules and polymeric materials contain alkyne structures or are synthesized from simple alkyne compounds. Therefore, a large number of methods for synthesizing alkyne derivatives came into being. |
use | for organic synthesis. |
production method | is obtained by brominating stilbene and then reacting with potassium hydroxide. |