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Key Documents

F15250

Sigma-Aldrich

2-Fluoropyridine

98%

Synonym(s):

2-Pyridyl fluoride

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About This Item

Empirical Formula (Hill Notation):
C5H4FN
CAS Number:
Molecular Weight:
97.09
Beilstein:
1515
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

refractive index

n20/D 1.466 (lit.)

bp

126 °C/753 mmHg (lit.)

density

1.128 g/mL at 25 °C (lit.)

SMILES string

Fc1ccccn1

InChI

1S/C5H4FN/c6-5-3-1-2-4-7-5/h1-4H

InChI key

MTAODLNXWYIKSO-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

75.2 °F - closed cup

Flash Point(C)

24 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Alessio Nicolini et al.
Inorganic chemistry, 57(9), 5438-5448 (2018-04-19)
The stringlike complex [Fe4(tpda)3Cl2] (2; H2tpda = N2, N6-bis(pyridin-2-yl)pyridine-2,6-diamine) was obtained as the first homometallic extended metal atom chain based on iron(II) and oligo-α-pyridylamido ligands. The synthesis was performed under strictly anaerobic and anhydrous conditions using dimesityliron, [Fe2(Mes)4] (1; HMes
Mohammad Hasani et al.
The journal of physical chemistry. B, 123(8), 1815-1821 (2019-02-20)
Protic ionic liquids (PILs) are made by proton transfer from a Brønsted acid to a base and are of interest for their solvent and electrolyte properties such as high ionic conductivity. Unfortunately, many PILs have been misnamed, because their ionic
Anna C Susa et al.
Journal of the American Society for Mass Spectrometry, 28(2), 332-340 (2016-10-14)
Factors that influence the charging of protein ions formed by electrospray ionization from aqueous solutions in which proteins have native structures and function were investigated. Protein ions ranging in molecular weight from 12.3 to 79.7 kDa and pI values from
The many roles for fluorine in medicinal chemistry.
William K Hagmann
Journal of medicinal chemistry, 51(15), 4359-4369 (2008-06-24)

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