347051
3-Fluorophenethylamine
99%
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About This Item
Linear Formula:
FC6H4CH2CH2NH2
CAS Number:
Molecular Weight:
139.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C8H10FN/c9-8-3-1-2-7(6-8)4-5-10/h1-3,6H,4-5,10H2
SMILES string
NCCc1cccc(F)c1
InChI key
AUCVZEYHEFAWHO-UHFFFAOYSA-N
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.)
functional group
amine, fluoro
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
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
181.4 °F - closed cup
flash_point_c
83 °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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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
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
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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