Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
FCH2CH2NH2 · HCl
CAS Number:
Molecular Weight:
99.54
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
207-302-3
MDL number:
Product Name
2-Fluoroethylamine hydrochloride, technical grade, 90%
InChI key
YRRZGBOZBIVMJT-UHFFFAOYSA-N
InChI
1S/C2H6FN.ClH/c3-1-2-4;/h1-2,4H2;1H
SMILES string
Cl.NCCF
grade
technical grade
assay
90%
form
solid
mp
99-103 °C (lit.)
functional group
amine
fluoro
Quality Level
Looking for similar products? Visit Product Comparison Guide
Application
2-Fluoroethylamine hydrochloride may be used in the synthesis of the following:
- 2-fluoroethylisocyanate
- 1,3-bis-(2-fluoroethyl) urea (BFU)
- N-2-fluoroethylmaleimide
- [Cu4(O)(Ln)2(CH3COO)4] where HL= 4-methyl-2,6-bis(2-fluoroethyliminomethyl) phenol
- 1-O-(4-(2-fluoroethyl-carbamoyloxymethyl)-2-nitrophenyl)-O-β-D-glucopyronuronate (FEAnGA)
General description
2-Fluoroethylamine hydrochloride is a fluorinated alkylammonium salt. Studies suggest that adding a fluorine atom to it leads to double gauche effect in the resulting 2,2-difluoroethylamine chloride. Microwave spectral studies for 2-fluoroethylamine has been conducted.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Tetranuclear copper (II)-Schiff-base complexes as active catalysts for oxidation of cyclohexane and toluene.
Roy P and Manassero M.
Dalton Transactions, 39(6), 1539-1545 (2010)
Microwave-spectrum, conformational equilibrium, intramolecular hydrogen-bonding, dipole-moments, N-14 nuclear-quadrupole coupling-constants and centrifugal-distortion constants of 2-fluoroethylamine.
Marstokk KM and Mollendal H.
Acta Chemica Scandinavica, 34(1), 15-29 (1980)
Conformational analysis of 2, 2-difluoroethylamine hydrochloride: double gauche effect.
Silla JM, et al.
Beilstein Journal of Organic Chemistry, 10(1), 877-882 (2014)
Development of a new thiol site-specific prosthetic group and its conjugation with [Cys40]-exendin-4 for in vivo targeting of insulinomas.
Yue X, et al.
Bioconjugate Chemistry, 24(7), 1191-1200 (2013)
Inês F Antunes et al.
Bioconjugate chemistry, 21(5), 911-920 (2010-04-27)
To increase the therapeutic index of chemotherapeutic drugs, prodrugs have been investigated as anticancer agents, as they may present fewer cytotoxic side effects than conventional cytotoxic drugs, while therapeutic efficacy is maintained or even increased. Extracellular beta-glucuronidase (beta-GUS) in the
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service