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Merck
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文件

193828

Sigma-Aldrich

茚

≥99%

别名:

Indonaphthene

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About This Item

经验公式（希尔记法）:
C9H8
CAS号:
95-13-6
分子量:
116.16
Beilstein:
635873
EC號碼:
202-393-6
MDL號碼:
MFCD00003777
分類程式碼代碼:
12352100
PubChem物質ID:
24851616
NACRES:
NA.22

品質等級

100

化驗

≥99%

形狀

liquid

折射率

n20/D 1.595 (lit.)

bp

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

溶解度

organic solvents: miscible
water: insoluble

密度

0.996 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

C1C=Cc2ccccc12

InChI

1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2

InChI 密鑰

YBYIRNPNPLQARY-UHFFFAOYSA-N

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相关类别

一般說明

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。

應用

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。

象形圖

FlameHealth hazard
GHS02,GHS08

訊號詞

Danger

危險聲明

H226,H304

危險分類

Asp. Tox. 1 - Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

136.4 °F - closed cup

閃點（°C）

58 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Hahn SF and Hillmyer MA.
Macromolecules, 36(1), 71-76 (2003)
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
David Schneider et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(50), 12243-12252 (2017-03-24)
A series of heteroleptic tris(cyclopentadienyl) Ce
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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