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347051

Sigma-Aldrich

3-Fluorophenethylamine

99%

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About This Item

Linear Formula:
FC6H4CH2CH2NH2
CAS Number:
404-70-6
Molecular Weight:
139.17
MDL number:
MFCD00075376
UNSPSC Code:
12352100
PubChem Substance ID:
24861461
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.509 (lit.)

bp

87 °C/15 mmHg (lit.)

density

1.066 g/mL at 25 °C (lit.)

SMILES string

NCCc1cccc(F)c1

InChI

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

InChI key

AUCVZEYHEFAWHO-UHFFFAOYSA-N

Application

3-Fluorophenethylamine may be used in the synthesis of:
  • N-(3-florophenyl)ethylcaffeamide and its anti-inflammatory activity was evaluated
  • N-{2-[(3-fluorophenyl)ethyl]}-2-methylpropanamide
  • N-(3′-fluorophenyl)ethyl-4-azahexacyclo[5.4.1.02,6.03,10.05,9.08,11]dodecan-3-ol

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

181.4 °F - closed cup

Flash Point(C)

83 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Jung-Chun Liao et al.
International journal of molecular sciences, 14(8), 15199-15211 (2013-07-28)
In this study, we evaluated the anti-inflammatory activity of one synthetic product, N-(3-Florophenyl)ethylcaffeamide (abbrev. FECA), by using animal model of λ-carrageenan-induced paw edema in mice. The anti-inflammatory mechanism of FECA was determined by measuring the levels of cyclooxygenase-2 (COX-2), nitric
Xiang Liu et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 1(1), 31-38 (2006-06-23)
Three new trishomocubane analogues based on the 4-azahexacyclo[5.4.1.0(2,6).0(3,10).0(5,9).0(8,11)] dodecane-3-ol skeleton have been synthesised and assessed for their affinities at both sigma-1 and sigma-2 receptors. The effect of various N-substitution on the polycyclic moiety was examined. All synthesised compounds displayed high
Susumu Watanuki et al.
Chemical & pharmaceutical bulletin, 59(8), 1029-1037 (2011-08-02)
A series of 1-isopropyl-1,2,3,4-tetrahydroisoquinoline derivatives were synthesized and their bradycardic activities were evaluated in isolated guinea pig right atria. Structure-activity relationship studies revealed that the introduction of an appropriate substituent and its position on the 1,2,3,4-tetrahydroisoquinoline ring are essential for

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