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Merck

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號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

technical grade

品質等級

化驗

≥90%

形狀

liquid

包含

50-100 ppm tert-butylcatechol as stabilizer

折射率

n20/D 1.595 (lit.)

bp

181-182 °C (lit.)

mp

−5-−3 °C (lit.)

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

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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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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)
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)
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
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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