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3-(Trifluoromethyl)benzylamine | CAS:2740-83-2
3-(Trifluoromethyl)benzylamine
  • Name:3-(Trifluoromethyl)benzylamine
  • CAS:2740-83-2
  • Synonyms:
  • Molecular Formula:C8H8F3N
  • Molecular Weight:175.15
  • EINESC:220-367-2

Description

Properties

Water Solubility Insoluble
Boiling point 93-97 ºC (22 mmHg)
Flash point 71 ºC
Density 1.222
Refractive index 1.462-1.464

Safety

Symbol(GHS) C
Hazard Codes R34
SDS/MSDS S26;S36/37/39;S45

SDS

Source SDS/MSDS Samples
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Articles
Peer-Reviewed Papers
Multivariate approach for the enantioselective analysis in micellar electrokinetic chromatography-mass spectrometry. I. Simultaneous optimization of binaphthyl derivatives in negative ion mode.Jun He et al.Journal of chromatography. A, 1216(5), 845-856 (2008-12-27) Dual organocatalysis: asymmetric allylic-allylic alkylation of alpha,alpha-dicyanoalkenes and Morita-Baylis-Hillman carbonates.Hai-Lei Cui et al.Chemistry (Weinheim an der Bergstrasse, Germany), 15(7), 1574-1577 (2009-01-10) Highly enantioselective phenylacetylene additions to ketones catalyzed by (S)-BINOL-Ti complex.Yifeng Zhou et al.Organic letters, 6(23), 4147-4149 (2004-11-05) Single diastereomers of unsymmetrical tris-spirocyclic cyclotriphosphazenes based on 1,1'-bi-2-naphthol--synthesis and structures.N N Bhuvan Kumar et al.Chirality, 20(6), 781-789 (2008-01-18) Use of multivariate analysis for optimization of separation parameters and prediction of migration time, resolution, and resolution per unit time in micellar electrokinetic chromatography.Alicia A Williams et al.Electrophoresis, 27(21), 4127-4140 (2006-11-01) Kelly, T. R.; Whiting, A.; Chandrakumar, N. S. Journal of the American Chemical Society, 108, 3510-3510 (1986) Highly selective recognition on enatioselective of R(+) and S(-)-1,1-Bi(2-naphthol) using of Eu(dap)3 complex as photo probe.Esam Bakir Journal of fluorescence, 22(3), 871-874 (2011-12-24) Analyte separation by OMNiMIPs imprinted with multiple templates.Jason Lejeune et al.Biosensors & bioelectronics, 25(3), 604-608 (2009-03-27) Study of the fluorescent properties of partially hydrogenated 1,1'-bi-2-naphthol-amine molecules and their use for enantioselective fluorescent recognition.Shanshan Yu et al.The Journal of organic chemistry, 76(8), 2814-2819 (2011-03-17) Heterocomplexation of a chiral dipeptide and quantitative enantiomeric enrichment of nonracemic 1,1'-bi-2-naphthol.Zixing Shan et al.The Journal of organic chemistry, 73(22), 9158-9160 (2008-10-23) Simple protocols for NMR analysis of the enantiomeric purity of chiral primary amines.Yolanda Pérez-Fuertes et al.Nature protocols, 3(2), 210-214 (2008-02-16) A highly sensitive water-soluble system to sense glucose in aqueous solution.Liheng Feng et al.Organic & biomolecular chemistry, 9(8), 2938-2942 (2011-03-08) Development of a continuous-flow system for asymmetric hydrogenation using self-supported chiral catalysts.Lei Shi et al.Chemistry (Weinheim an der Bergstrasse, Germany), 15(38), 9855-9867 (2009-08-18) Use of NMR binding interaction mapping techniques to examine interactions of chiral molecules with molecular micelles.Kevin F Morris et al.The journal of physical chemistry. B, 110(35), 17359-17369 (2006-09-01) BINOL: a versatile chiral reagent.Jean Michel Brunel Chemical reviews, 105(3), 857-897 (2005-03-10) The use of poly(sodium N-undecanoyl-L-leucylvalinate), poly(sodium N-undecanoyl-L-leucinate) and poly(sodium N-undecanoyl-L-valinate) surfactants as chiral selectors for determination of enantiomeric composition of samples by multivariate regression modeling of fluorescence spectral data.Sayo O Fakayode et al.Journal of fluorescence, 16(5), 659-670 (2006-07-11) Multi-analyte imprinting capability of OMNiMIPs versus traditional molecularly imprinted polymers.Andrew C Meng et al.Journal of molecular recognition : JMR, 22(2), 121-128 (2009-02-06) Chromatographic enantioseparations of binaphthyl compounds on an immobilized polysaccharide-based chiral stationary phase.Wen Weng et al.Journal of chromatography. A, 1210(2), 178-184 (2008-10-07) Solvent effect in the chromatographic enantioseparation of 1,1'-bi-2-naphthol on a polysaccharide-based chiral stationary phase.Fengping Zhan et al.Journal of chromatography. A, 1217(26), 4278-4284 (2010-05-15) Temperature-induced inversion of elution order in the chromatographic enantioseparation of 1,1'-bi-2-naphthol on an immobilized polysaccharide-based chiral stationary phase.Bixia Yao et al.Journal of chromatography. A, 1216(28), 5429-5435 (2009-06-09) Toward chiral sum-frequency spectroscopy.Na Ji et al.Journal of the American Chemical Society, 128(27), 8845-8848 (2006-07-06) Evaluation of co-solvent fraction, pressure and temperature effects in analytical and preparative supercritical fluid chromatography.Dennis Åsberg et al.Journal of chromatography. A, 1374, 254-260 (2014-12-17) Chiral separation of 1,1'-bi-2-naphthol and its analogue on molecular imprinting monolithic columns by HPLC.Junjie Ou et al.Journal of separation science, 28(17), 2282-2287 (2005-12-14) UV near-resonance Raman spectroscopic study of 1,1'-bi-2-naphthol solutions.Zun-yun Li et al.The journal of physical chemistry. A, 111(22), 4767-4775 (2007-05-16) Synthesis and application of modular phosphine-phosphoramidite ligands in asymmetric hydroformylation: structure-selectivity relationship.Xiaowei Zhang et al.Chemistry (Weinheim an der Bergstrasse, Germany), 16(3), 871-877 (2009-12-02) Studies of the resolution of racemic 1,1'-bi-2-naphthol with a dipeptide chiral selector identified from a small library.Junmin Huang et al.Journal of chromatography. A, 1102(1-2), 176-183 (2005-11-04) Monolayers of twisted binaphthyls for aromatic crystallization at low nucleation densities and high growth rates.Sang-Mi Jeong et al.Journal of the American Chemical Society, 130(11), 3497-3501 (2008-02-22) Optimization of 12 chiral analytes with 8 polymeric surfactants.Eugene Billiot et al.Journal of chromatographic science, 46(9), 757-763 (2008-11-15) Sasai, H.; Arai, T. et al. Journal of the American Chemical Society, 117, 6194-6194 (1995)
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