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Sigma-Aldrich

2-Fluorophenethylamine

99%

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About This Item

Linear Formula:
FC6H4CH2CH2NH2
CAS Number:
Molecular Weight:
139.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.51 (lit.)

bp

64 °C/0.6 mmHg (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

NCCc1ccccc1F

InChI

1S/C8H10FN/c9-8-4-2-1-3-7(8)5-6-10/h1-4H,5-6,10H2

InChI key

RIKUOLJPJNVTEP-UHFFFAOYSA-N

General description

2-Fluorophenethylamine is an amine.

Application

2-Fluorophenethylamine may be used in the synthesis of ethyl 2-cyano-3-(N-2-fluorophenethylamino)-3-methythioacrylate. It may be used for the derivatization of methoxybenzaldehyde polystyrene resin.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis and bioactivity of Ethyl 2-Cyano-3-methylthio-3-(N-2-Fluorophenethylamino) Acrylates.
ZHOU J-K, et al.
Journal of Guizhou Educational Institute, 017-017 (2007)
S L Dax et al.
Current medicinal chemistry, 6(3), 255-270 (1999-04-29)
Solid-phase organic synthesis, particularly when used in conjunction with combinatorial techniques, is emerging as a revolutionary technology in chemistry. Multi-component reaction systems are particularly valued because several elements of diversity can be introduced in a single transformation thereby expanding the
Daniel B Straus et al.
ACS nano, 14(3), 3621-3629 (2020-03-03)
We report a family of two-dimensional hybrid perovskites (2DHPs) based on phenethylammonium lead iodide ((PEA)2PbI4) that show complex structure in their low-temperature excitonic absorption and photoluminescence (PL) spectra as well as hot exciton PL. We replace the 2-position (ortho) H

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