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Merck
CN

I2800

Sigma-Aldrich

contains 50-100 ppm tert-butylcatechol as stabilizer, technical grade, ≥90%

别名:

Indonaphthene

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About This Item

经验公式(希尔记法):
C9H8
CAS号:
分子量:
116.16
Beilstein:
635873
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

technical grade

质量水平

方案

≥90%

表单

liquid

包含

50-100 ppm tert-butylcatechol as stabilizer

折射率

n20/D 1.595 (lit.)

沸点

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

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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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

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分析证书(COA)

Lot/Batch Number

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访问文档库

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
Two-step synthesis of stable dioxadicarbaporphyrins from bis(3-indenyl)methane.
Timothy D Lash et al.
Angewandte Chemie (International ed. in English), 51(43), 10871-10875 (2012-09-25)
Adam C Glass et al.
Organic letters, 10(21), 4855-4857 (2008-10-07)
A new methodology for the preparation of substituted naphthalenes starting from readily available indenones, organometal reagents, and trimethylsilyldiazomethane via a catalytic rearrangement process is described. Hindered biaryl naphthalenes, including triortho-substituted biaryls, can be accessed through our method. Our results are
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)
Cobalt-catalyzed regioselective synthesis of indenamine from o-iodobenzaldimine and alkyne: intriguing difference to the nickel-catalyzed reaction.
Chuan-Che Liu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(31), 9503-9506 (2008-09-24)

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