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368032

Sigma-Aldrich

2-Fluorophenethylamine

99%

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About This Item

Linear Formula:
FC6H4CH2CH2NH2
CAS Number:
52721-69-4
Molecular Weight:
139.17
MDL number:
MFCD00075502
UNSPSC Code:
12352100
PubChem Substance ID:
24862880
NACRES:
NA.22

Quality Level

100

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

Related Categories

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
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

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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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
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)

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