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| 1,4-DIPHENYLBUTADIYNE Basic information |
Product Name: | 1,4-DIPHENYLBUTADIYNE | Synonyms: | (4-Phenyl-1,3-butadiynyl)benzene;1,1’-(1,3-butadiyne-1,4-diyl)bis-benzen;1,1’-(1,3-butadiyne-1,4-diyl)bisbenzene;1,4-Diphenyl-1,3-butadiyne;1,4-Diphenylbut-1,3-diyne;benzene,1,1’-(1,3-butadiyne-1,4-diyl)bis-;Butadiyne, diphenyl-;NSC 529170 | CAS: | 886-66-8 | MF: | C16H10 | MW: | 202.25 | EINECS: | 212-953-1 | Product Categories: | Building Blocks;Chemical Synthesis;Organic Building Blocks;Aromatic Hydrocarbons (substituted) & Derivatives;Acetylenes;Acetylenic Hydrocarbons having Benzene Ring;Alkynes;Internal;Organic Building Blocks | Mol File: | 886-66-8.mol | |
| 1,4-DIPHENYLBUTADIYNE Chemical Properties |
Melting point | 86-87 °C (lit.) | Boiling point | 210 °C / 3mmHg | density | 1.2615 (estimate) | refractive index | 1.5000 (estimate) | storage temp. | Sealed in dry,Room Temperature | form | powder to crystal | color | White to Light yellow | Water Solubility | Sparingly soluble in water(5.5E-4 g/L) (25°C). Soluble in toluene almost transparency. | BRN | 1910105 | CAS DataBase Reference | 886-66-8(CAS DataBase Reference) | EPA Substance Registry System | Benzene, 1,1'-(1,3-butadiyne-1,4-diyl)bis- (886-66-8) |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-37/39 | WGK Germany | 3 | HS Code | 29029090 |
| 1,4-DIPHENYLBUTADIYNE Usage And Synthesis |
Chemical Properties | white crystalline needles | Uses | 1,4-Diphenylbutadiyne was used in the preparation of 7,8-dehydropurpurin dimers via two-fold Pd-catalyzed [3+2] annulation of meso-bromoporphyrin. | Definition | ChEBI: 1,4-diphenylbutadiyne is an arylacetylene and a member of benzenes. It has a role as a fluorochrome. | Synthesis Reference(s) | The Journal of Organic Chemistry, 52, p. 443, 1987 DOI: 10.1021/jo00379a025 Synthetic Communications, 20, p. 2181, 1990 DOI: 10.1080/00397919008053156 Tetrahedron Letters, 26, p. 523, 1985 DOI: 10.1016/S0040-4039(00)61928-7 | General Description | 1,4-Diphenylbutadiyne reacts with [WI2(CO)3(NCMe)2] in CH2Cl2 to give the iodo-bridged dimer [W(μ-I)I(CO)(NCMe)(η2PhC2C2Ph)]2. 1,4-Diphenylbutadiyne on UV irradiation with olefins such as 2,3-dimethyl-2-butene, 1,4-cyclohexadiene and dimethyl fumarate yields cross-cycloaddition products. |
| 1,4-DIPHENYLBUTADIYNE Preparation Products And Raw materials |
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