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Merck

519405

Sigma-Aldrich

1-Ethinyl-3-fluorbenzol

98%

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5 G
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5 G
€ 120,00

About This Item

Lineare Formel:
FC6H4C≡CH
CAS-Nummer:
Molekulargewicht:
120.12
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

€ 120,00


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Assay

98%

Brechungsindex

n20/D 1.5170 (lit.)

bp

138 °C (lit.)

Dichte

1.039 g/mL at 25 °C (lit.)

Funktionelle Gruppe

fluoro

SMILES String

Fc1cccc(c1)C#C

InChI

1S/C8H5F/c1-2-7-4-3-5-8(9)6-7/h1,3-6H

InChIKey

PTRUTZFCVFUTMW-UHFFFAOYSA-N

Piktogramme

FlameExclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

90.0 °F - closed cup

Flammpunkt (°C)

32.2 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Ya Zhou et al.
Probe Reports from the NIH Molecular Libraries Program, 2011 Oct 31 (Updated 2013 Mar 7) (2013-06-14)
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Jason Manka et al.
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Allosteric modulators for G-protein-coupled receptors (GPCRs) provide numerous advantages over orthosteric ligands, including greater sub-type selectivity, reduced receptor desensitization, saturability of effect, and potential for enhanced therapeutic index. Positive allosteric modulators (PAMs) of the group I metabotropic glutamate receptor mGlu
Chunfa Xu et al.
Angewandte Chemie (International ed. in English), 53(35), 9316-9320 (2014-07-22)
A new, electrophilic trifluoromethylthiolating reagent, N-trifluoromethylthiosaccharin, was developed and can be synthesized in two steps from saccharin within 30 minutes. N-trifluoromethylthiosaccharin is a powerful trifluoromethylthiolating reagent and allows the trifluoromethylthiolation of a variety of nucleophiles such as alcohols, amines, thiols, electron-rich

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