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I2800

Indene

Name: Indene
Brand: ALDRICH

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

Synonym(s):

Indonaphthene

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About This Item

Empirical Formula (Hill Notation):

C₉H₈

CAS Number:

95-13-6

Molecular Weight:

116.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896009

EC Number:

202-393-6

Beilstein/REAXYS Number:

635873

MDL number:

MFCD00003777

Assay:

≥90%

Form:

liquid

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Properties

grade

technical grade

Quality Level

100

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

SMILES string

C1C=Cc2ccccc12

InChI

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

InChI key

YBYIRNPNPLQARY-UHFFFAOYSA-N

Description

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pictograms

GHS02,GHS08

signalword

Danger

hcodes

H226,H304

pcodes

P210 - P233 - P240 - P241 - P301 + P310 - P331

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 3

Storage Class

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

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In vitro evolution of styrene monooxygenase from Pseudomonas putida CA-3 for improved epoxide synthesis.

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)

Indene-based scaffolds. 2. An indole-indene switch: discovery of novel indenylsulfonamides as 5-HT6 serotonin receptor agonists.

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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Global Trade Item Number

SKU	GTIN
I2800-1L	04061838137210
I2800-250ML	04061838137227