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Merck
CN

361828

4-Fluorophenethylamine

99%

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About This Item

Linear Formula:
FC6H4CH2CH2NH2
CAS Number:
1583-88-6
Molecular Weight:
139.17
NACRES:
NA.22
PubChem Substance ID:
24862263
UNSPSC Code:
12352100
EC Number:
216-435-6
MDL number:
MFCD00134208
Assay:
99%
Form:
liquid

Key Documents

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Product Name

4-Fluorophenethylamine, 99%

InChI key

CKLFJWXRWIQYOC-UHFFFAOYSA-N

InChI

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

SMILES string

NCCc1ccc(F)cc1

assay

99%

form

liquid

refractive index

n20/D 1.5072 (lit.)

bp

50-52 °C/0.15 mmHg (lit.)

density

1.061 g/mL at 25 °C (lit.)

functional group

amine
fluoro

Gene Information

human ... AOC3(8639)
mouse ... Aoc3(11754)

Application

4-Fluorophenethylamine may be employed as nucleophile in the synthesis of 2-amino-4-arylpyrimidine derivatives. It is suitable for use in the preparation of ortho-metalated primary phenethylamines having electron-releasing and electron-withdrawing groups on the aromatic ring, leading to complexes containing six membered palladacycles.

pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

174.2 °F - closed cup

flash_point_c

79 °C - closed cup

ppe

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

Regulatory Information

监管及禁止进口产品
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Certificates of Analysis (COA)

Lot/Batch Number
SHBH5022V
SHBB3020V
24996EMV
24996EM
18425LH

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Mitra Matloobi et al.
Journal of combinatorial chemistry, 9(2), 275-284 (2007-03-14)
An efficient and rapid microwave-assisted solution-phase method for the synthesis of 2-amino-4-arylpyrimidine-5-carboxylic acid derivatives has been developed. The five-step linear protocol involves an initial Biginelli multicomponent reaction leading to dihydropyrimidine-2-thiones which are subsequently S-alkylated with methyl iodide. The resulting 2-methylthiodihydropyrimidines
Ortho-metalated primary amines. 6.1 The first synthesis of six-membered palladacycles from primary amines containing electron-withdrawing substituents: end of the limiting rules of Cope and Friedrich on cyclopalladation of benzyl-and phenethylamines.
Vicente J, et al.
Organometallics, 22(26), 5513-5517 (2003)
Tianqi Niu et al.
Nano letters, 19(10), 7181-7190 (2019-09-04)
Perovskite solar cells based on two-dimensional/three-dimensional (2D/3D) hierarchical structure have attracted significant attention in recent years due to their promising photovoltaic performance and stability. However, obtaining a detailed understanding of interfacial mechanism at the 2D/3D heterojunction, for example, the ligand-chemistry-dependent

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