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Merck
CN

168769

Sigma-Aldrich

98%

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
Beilstein:
635873
EC 号:
MDL编号:
UNSPSC代码:
12352100
eCl@ss:
39011614
PubChem化学物质编号:
NACRES:
NA.22
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质量水平

方案

98%

表单

liquid

折射率

n20/D 1.595 (lit.)

沸点

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

溶解性

organic solvents: miscible
water: insoluble

密度

0.996 g/mL at 25 °C (lit.)

储存温度

2-8°C

SMILES字符串

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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一般描述

通过 恶臭假单胞菌 红球菌 将茚氧化为 顺式 -和 反式 -茚满二醇及相关代谢产物的混合物。

应用

茚用于合成新的 C 60 衍生物茚-C 60 双加合物 。在 CH 2 Cl 2 中,用甲基异丙醚/TiCl 4 引发控制阳离子聚合制备聚茚。

象形图

FlameHealth hazard

警示用语:

Danger

危险声明

危险分类

Asp. Tox. 1 - Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

136.4 °F - closed cup

闪点(°C)

58 °C - closed cup

个人防护装备

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
High glass transition temperature polyolefins obtained by the catalytic hydrogenation of polyindene.
Hahn SF and Hillmyer MA.
Macromolecules, 36(1), 71-76 (2003)
Youjun He et al.
Journal of the American Chemical Society, 132(4), 1377-1382 (2010-01-09)
Polymer solar cells (PSCs) are commonly composed of a blend film of a conjugated polymer donor and a soluble C(60) derivative acceptor sandwiched between an ITO anode and a low-workfunction metal cathode. Poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C-61-butyric acid methyl ester (PCBM)
Lucas J Gursky et al.
Applied microbiology and biotechnology, 85(4), 995-1004 (2009-07-02)
The styAB genes from Pseudomonas putida CA-3, which encode styrene monooxygenase, were subjected to three rounds of in vitro evolution using error-prone polymerase chain reaction with a view to improving the rate of styrene oxide and indene oxide formation. Improvements
Regioselective synthesis of indenols by rhodium-catalyzed C-H activation and carbocyclization of aryl ketones and alkynes.
Krishnamoorthy Muralirajan et al.
Angewandte Chemie (International ed. in English), 50(18), 4169-4172 (2011-03-31)

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