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Merck
CN

I2800

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

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:
Assay:
≥90%
Form:
liquid
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SMILES string

C1C=Cc2ccccc12

InChI key

YBYIRNPNPLQARY-UHFFFAOYSA-N

InChI

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

grade

technical grade

assay

≥90%

form

liquid

contains

50-100 ppm tert-butylcatechol as stabilizer

refractive index

n20/D 1.595 (lit.)

bp

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

density

0.996 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

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pictograms

FlameHealth hazard

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

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分析证书(COA)

Lot/Batch Number

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Timothy D Lash et al.
Angewandte Chemie (International ed. in English), 51(43), 10871-10875 (2012-09-25)
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)
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
Dorian S N Parker et al.
Chemistry, an Asian journal, 6(11), 3035-3047 (2011-10-01)
Polycyclic aromatic hydrocarbons (PAHs) are regarded as key intermediates in the molecular growth process that forms soot from incomplete fossil fuel combustion. Although heavily researched, the reaction mechanisms for PAH formation have only been investigated through bulk experiments; therefore, current

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