Introdução de Produto

1,2-Hydrindene;1H-Indene, 2,3-dihydro-;INDANE OEKANAL, 250 MG;Indane,95%;1,2-dihydroindene;Indan Odor Standard;Hydrinden;Bicyclo[4.3.0]nona-1,3,5-triene
496-11-7
C9H10
118.18
207-814-7
 
496-11-7.mol
Indan Structure
 
-51 degree (lit.)
176 degree (lit.)
0.965 g/mL at 25 degree (lit.)
1.5 at 25 degree (extrapolated, Ambrose and Sprake, 1975)
n20/D 1.537(lit.)
50 degree
Soluble in alcohol, ether (Weast, 1986), and many aliphatic hydrocarbons (hexane, pentane), and aromatic hydrocarbons (benzene)
>14 (Schwarzenbach et al., 1993)
0.0037ppm
14,4931
1904376
(x 10-33/mol): 2.14 at 25 degree (approximate - calculated from water solubility and vapor pressure)
PQNFLJBBNBOBRQ-UHFFFAOYSA-N
496-11-7(CAS DataBase Reference)
Indan (496-11-7)
 
10-65
23-24/25-62
UN 3295 3/PG 3
3
NK3750000
3
29029090
 
 
ChEBI: Indane is an ortho-fused bicyclic hydrocarbon consisting of a benzene ring fused to a cyclopentane ring; a high-boiling (176 degree ) colourless liquid. It is a member of indanes and an ortho-fused bicyclic hydrocarbon.
Indane is used as anti-vibration agent for aviation fuel and anti-vibration agent for rubber industry. Its derivatives can be used in pharmaceuticals and solvents. Indane can be cracked to produce benzene compounds.
Taking heavy benzene with a Indan content of 35% as a raw material, rectifying it through an emulsification tower, and cutting the 182 degree fraction from the top of the tower, that is, Indan with a content of more than 90%.?
Journal of the American Chemical Society, 111, p. 314, 1989 10.1021/ja00183a048
The Journal of Organic Chemistry, 41, p. 1184, 1976 10.1021/jo00869a022
3-phenyl-1-propene is isomerized to give indane in the presence of AlCl3:
Synthesis_496-11-7
Detected in distilled water-soluble fractions of 87 octane gasoline (0.40 mg/L), 94 octane gasoline (0.23 mg/L), Gasohol ({{10}}.50 mg/L), No. 2 fuel oil (0.05 mg/L), jet fuel A (0.15 mg/L), and diesel fuel (0.06 mg/L) (Potter, 1996). Based on laboratory analysis of 7 coal tar samples, indan concentrations ranged from ND to 3,800 ppm (EPRI, 1970).
Gas-phase reaction rate constants for OH radicals, NO3 radicals, and ozone at 24 degree were 1.9 x 10-11, 6.6 x 10-15<3 x 10-193/molecule?sec, respectively (Kwok et al., 1997).
Shake indane with conc H2SO4, then water, dry and fractionally distil it. [Beilstein 5 H 486, 5 I 234, 5 II 376, 5 III 1200, 5 IV 1371.]
 
Indene-->
1,2-DIMETHYLCYCLOHEXANE-->4-INDANOL-->4-AMINOINDAN-->5-INDANOL-->N-PROPYLBENZENE-->N-(Bromomethyl)phthalimide-->1,2,3,5,6,7-Hexahydro-s-indacene-4-acetic acid-->INDANE-5-SULFONYL CHLORIDE-->2-CHLORO-1-(2,3-DIHYDRO-1H-INDEN-5-YL)ETHANONE

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