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About This Item
Linear Formula:
FC6H4CH2NH2
CAS Number:
Molecular Weight:
125.14
Beilstein:
636501
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39040409
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.512 (lit.)
bp
183 °C (lit.)
density
1.095 g/mL at 25 °C (lit.)
functional group
amine
fluoro
SMILES string
NCc1ccc(F)cc1
InChI
1S/C7H8FN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2
InChI key
IIFVWLUQBAIPMJ-UHFFFAOYSA-N
Gene Information
human ... AOC3(8639)
mouse ... Aoc3(11754)
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General description
[18F]4-fluorobenzylamine reacts with the α- and γ-carboxyl groups of folic acid to yield 18F-labeled folate. It is an important building block for the synthesis of 18F-labeled compounds.
Application
4-Fluorobenzylamine was used in the synthesis of new tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
150.8 °F - closed cup
Flash Point(C)
66 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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T Haradahira et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 49(12), 1551-1556 (1998-09-24)
A fluorine-18 labeled analog of an antitumor prostaglandin delta 7-PGA1 methyl ester, 15-deoxy-13,14-dihydro-delta 7-PGA1 4-[18F]fluorobenzyl amide ([18F]3), was synthesized as a tracer candidate for detecting tumors with positron emission tomography. p-[18F]Fluorobenzylamine (p-[18F]FBnA) used as a labeled precursor for the synthesis
Ingrid Koslowsky et al.
Organic & biomolecular chemistry, 8(20), 4730-4735 (2010-08-27)
A novel synthesis of 4-[(18)F]fluorobenzylamine ([(18)F]FBA) by means of transition metal-assisted sodium borohydride reduction of 4-[(18)F]fluorobenzonitrile ([(18)F]FBN) is described. This approach could successfully be extended to borohydride exchange resin (BER) enabling a viable option for use in automated syntheses. [(18)F]FBA
Walkiria Schlindwein et al.
Dalton transactions (Cambridge, England : 2003), (10)(10), 1313-1321 (2006-03-01)
New tris-iron(III) chelates of 3-hydroxy-4-pyridinone ligands derived from maltol (3-hydroxy-2-methyl-4-pyrone) or ethylmaltol (2-ethyl-3-hydroxy-4-pyrone), including a variety of N-aryl (phenyl, 4'-tolyl, 4'-(n-butyl)phenyl, 4'-(n-hexyl)phenyl) and N-benzyl (4'-methylbenzyl, 4'-fluorobenzyl and 4'-(trifluoromethyl)benzylamine) substituents on the nitrogen atom of the pyridinone ring, have been prepared.
Guoqing Cheng et al.
ACS applied materials & interfaces, 12(15), 18084-18090 (2020-03-25)
Stability is becoming a main issue for perovskite light-emitting diodes (PeLEDs), as their external quantum efficiency (EQE) has been boosted to above 20%. An all-inorganic perovskite, cesium lead iodide (CsPbI3), has better stability than organic-inorganic hybrid perovskites but suffers from
Muhammad Kaleem Khosa et al.
Pakistan journal of pharmaceutical sciences, 28(6), 2167-2171 (2015-12-08)
New series of benzophenone imines with general formula Ph2-C=NR; R = Benzyl, 4-Fluorobenzyl, Naphthyl, Phenyl, 4-Nitrophenyl were synthesized by condensation of dichlorodiphenylmethane and different aromatic primary amines (1:1) Those imines were characterized by different physiochemical and spectroscopic techniques like melting
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