56930
Indene
technical, ≥90% (GC)
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About This Item
Empirical Formula (Hill Notation):
C9H8
CAS Number:
Molecular Weight:
116.16
EC Number:
202-393-6
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
635873
grade
technical
assay
≥90% (GC)
refractive index
n20/D 1.569, n20/D 1.595 (lit.)
bp
181-182 °C (lit.)
mp
−5-−3 °C (lit.)
density
0.996 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C1C=Cc2ccccc12
InChI
1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
InChI key
YBYIRNPNPLQARY-UHFFFAOYSA-N
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General description
may contain 1-2% benzonitrile
signalword
Danger
hcodes
pcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Ermitas Alcalde et al.
Journal of medicinal chemistry, 52(3), 675-687 (2009-01-23)
Scaffold selection involving an indole-to-indene core change led to the discovery of a series of indenylsulfonamides that act as 5-HT6 serotonin receptor agonists. The variety of the targeted ligands and their synthetic complexity required multistep synthetic approaches. The novel indenylsulfonamides
Helga Seyler et al.
The Journal of organic chemistry, 76(9), 3551-3556 (2011-03-12)
Various fullerene-based electron acceptor materials for organic photovoltaic applications were prepared via [3+2] and [4+2] cycloadditions using a continuous flow approach. The 1,3-dipolar cycloaddition of the tosylhydrazone precursor and the Diels-Alder cycloaddition of indene to either C(60) or C(70) under
Ermitas Alcalde et al.
Organic & biomolecular chemistry, 6(20), 3795-3810 (2008-10-10)
A series of novel indene derivatives designed by a scaffold selection gave access to several examples of (Z)-arylmethylideneindenes and indenylsulfonamides that acted as serotonin 5-HT(6) receptor ligands. Different synthetic multistep routes could be applied to these target compounds, each with
Hiroaki Kurouchi et al.
Journal of the American Chemical Society, 132(2), 807-815 (2009-12-19)
The chemical features, such as substrate stability, product distribution, and substrate generality, and the reaction mechanism of Brønsted superacid-catalyzed cyclization reactions of aromatic ring-containing acetoacetates (beta-ketoesters) were examined in detail. While two types of carbonyl cyclization are possible, i.e., keto
Song Tu et al.
Journal of agricultural and food chemistry, 56(13), 5247-5253 (2008-06-13)
Nineteen novel indene-substituted oxime ether strobilurins, which used an indene group to stabilize the ( E)-styryl group in SYP-Z071 (an unsaturated oxime strobilurin fungicide under development by the Shenyang Research Institute of Chemical Industry), were designed and synthesized. The biological
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