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Merck
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重要文件

168769

Sigma-Aldrich

98%

同義詞:

Indonaphthene

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About This Item

經驗公式(希爾表示法):
C9H8
CAS號碼:
分子量::
116.16
Beilstein:
635873
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
eCl@ss:
39011614
PubChem物質ID:
NACRES:
NA.22
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品質等級

化驗

98%

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

尋找類似的產品? 前往 產品比較指南

一般說明

通过 恶臭假单胞菌 红球菌 [1] 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。

應用

茚用于合成新的 C 60 衍生物茚-C 60 双加合物 [2]。在 CH 2 Cl 2 [3] 中,用甲基异丙醚/TiCl 4 引发控制阳离子聚合制备聚茚。

象形圖

FlameHealth hazard

訊號詞

Danger

危險聲明

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
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)
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

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