193828
茚
≥99%
别名:
Indonaphthene
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关于此项目
经验公式（希尔记法）:
C9H8
化学文摘社编号:
分子量:
116.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-393-6
Beilstein/REAXYS Number:
635873
MDL number:
eCl@ss:
39011614
Assay:
≥99%
Form:
liquid
InChI key
YBYIRNPNPLQARY-UHFFFAOYSA-N
InChI
1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
SMILES string
C1C=Cc2ccccc12
assay
≥99%
form
liquid
refractive index
n20/D 1.595 (lit.)
bp
181-182 °C (lit.)
mp
−5-−3 °C (lit.)
solubility
organic solvents: miscible, water: insoluble
density
0.996 g/mL at 25 °C (lit.)
storage temp.
2-8°C
Quality Level
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General description
恶臭假单胞菌和红球菌将茚氧化为顺式和反式茚满醇和相关代谢物的混合物。
Application
茚被用于合成新的 C60 衍生物，茚-C60 双加合物。通过在 CH2Cl2 中的异丙基甲烷/TiCl4引发的受控阳离子聚合，将其用于制备聚茚。
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 3
存储类别
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
法规信息
危险化学品
此项目有
High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Hahn SF and Hillmyer MA.
Macromolecules, 36(1), 71-76 (2003)
David Schneider et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(50), 12243-12252 (2017-03-24)
A series of heteroleptic tris(cyclopentadienyl) Ce
B C Buckland et al.
Metabolic engineering, 1(1), 63-74 (2000-08-10)
Indene is oxidized to mixtures of cis- and trans-indandiols and related metabolites by Pseudomonas putida and Rhodococcus sp. isolates. Indene metabolism is consistent with monooxygenase and dioxygenase activity. P. putida resolves enantiomeric mixtures of cis-1,2-indandiol by further selective oxidation of
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.
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
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