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  2. meso-Stilbene dibromide - Wikipedia

    en.wikipedia.org/wiki/Meso-stilbene_dibromide

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  3. (E)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(E)-Stilbene

    Cis-stilbene is a liquid at room temperature (melting point: 5–6 °C (41–43 °F)), while trans-stilbene is a crystalline solid which does not melt until around 125 °C (257 °F), illustrating the two isomers have significantly different physical properties. [5] [6]

  4. (Z)-Stilbene - Wikipedia

    en.wikipedia.org/wiki/(Z)-Stilbene

    Z)-Stilbene has a melting point of 5–6 °C (41–43 °F), while (E)-stilbene melts around 125 °C (257 °F), illustrating that the two compounds are quite different. Uses [ edit ]

  5. Diphenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Diphenylacetylene

    Melting point: 62.5 °C (144.5 °F; 335.6 K) Boiling point: 170 °C (338 °F; 443 K) at 19 mmHg Solubility in water. Insoluble Structure Dipole moment. 0 D:

  6. 1,4-Dibromobenzene - Wikipedia

    en.wikipedia.org/wiki/1,4-Dibromobenzene

    Melting point: 87 °C (189 °F; 360 K) [3] Boiling point: 220.4 °C (428.7 °F; 493.5 K) [3] Solubility in water. Practically insoluble [2] Solubility in other solvents

  7. Resveratrol - Wikipedia

    en.wikipedia.org/wiki/Resveratrol

    C 14 H 12 O 3: Molar mass: 228.247 g·mol −1 : Appearance white powder with slight yellow cast Melting point: 261 to 263 °C (502 to 505 °F; 534 to 536 K) [2] Solubility in water: 0.03 g/L

  8. Bibenzyl - Wikipedia

    en.wikipedia.org/wiki/Bibenzyl

    Melting point: 52.0 to 52.5 °C (125.6 to 126.5 °F; 325.1 to 325.6 K) [1] Boiling point: 284 °C (543 °F; 557 K) [1] Solubility in water. Insoluble

  9. 2,2,4,4-Tetramethyl-1,3-cyclobutanediol - Wikipedia

    en.wikipedia.org/wiki/2,2,4,4-Tetramethyl-1,3-cy...

    2,2,4,4-Tetramethyl-1,3-cyclobutanediol (CBDO) is an aliphatic diol.This diol is produced as a mixture of cis- and trans-isomers, depending on the relative stereochemistry of the hydroxyl groups.