Boiling point	-18 ºC

Symbol(GHS)	F
Hazard Codes	R11
SDS/MSDS	S16;S38

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
Apollo	View & Download

Synthetic Route

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Articles

Peer-Reviewed Papers

Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.Vincent Coeffard et al.The Journal of organic chemistry, 74(16), 5822-5838 (2009-07-10) Carbon position-specific isotope analysis of alanine and phenylalanine analogues exhibiting nonideal pyrolytic fragmentation.Christopher J Wolyniak et al.Analytical chemistry, 77(6), 1746-1752 (2005-03-15) D-alaninol adsorption on Cu(100): photoelectron spectroscopy and first-principles calculations.Paola Gori et al.The journal of physical chemistry. B, 112(13), 3963-3970 (2008-03-11) Transformation of isopropylamine to L-alaninol by Pseudomonas sp. strain KIE171 involves N-glutamylated intermediates.Susana I de Azevedo Wäsch et al.Applied and environmental microbiology, 68(5), 2368-2375 (2002-04-27) Synthesis of 1,3-diacylaminopropan-2-ols and corresponding 2-acyl derivatives as amide isosteres of natural lipids.F Mergen et al.Chemistry and physics of lipids, 59(3), 267-272 (1991-10-01) 2-amino-1-propanol versus 1-amino-2-propanol: valence band and C 1s core-level photoelectron spectra.D Catone et al.The Journal of chemical physics, 127(14), 144312-144312 (2007-10-16) Tetrahedron Asymmetry, 4, 1785-1785 (1993) Straightforward synthesis of enantiopure (R)- and (S)-trifluoroalaninol.Julien Pytkowicz et al.Organic & biomolecular chemistry, 8(20), 4540-4542 (2010-09-08) Chiral oxidovanadium (V) complexes with tridentate Schiff bases derived from S (+)-2-amino-1-propanol: Synthesis, structure, characterization and catalytic activity.Romanowski G and Lis T. Inorgorganica Chimica Acta, 394, 627-634 (2013) Towards the Determination of the Absolute Configuration of Complex Molecular Systems: Matrix Isolation Vibrational Circular Dichroism Study of (R)-2-Amino-1-propanol.Tarczay G, et al. Angewandte Chemie (International Edition in English), 45(11), 1775-1777 (2006) Tetrahedron Letters, 34, 7725-7725 (1993) The substrate-dependent steric course of the ethanolamine ammonia-lyase reaction.P Diziol et al.European journal of biochemistry, 106(1), 211-224 (1980-05-01) Tetrahedron Letters, 34, 3149-3149 (1993) Fluorescence sensing of ammonium and organoammonium ions with tripodal oxazoline receptors.Kyo Han Ahn et al.Organic letters, 5(9), 1419-1422 (2003-04-26) Thermal study of simple amino-alcohol solutions.Anne Baudot et al.Cryobiology, 44(2), 150-160 (2002-08-02) Modulation of acetylcholine release in rat hippocampus by amino alcohols and Bay K 8644.J R Bostwick et al.Brain research, 629(1), 79-87 (1993-11-26) How coenzyme B12-dependent ethanolamine ammonia-lyase deals with both enantiomers of 2-amino-1-propanol as substrates: structure-based rationalization.Naoki Shibata et al.Biochemistry, 50(4), 591-598 (2010-12-15) A colorimetric chiral sensor based on chiral crown ether for the recognition of the two enantiomers of primary amino alcohols and amines.Eun Na Rae Cho et al.Chirality, 23(4), 349-353 (2011-03-09) Analysis of the electron paramagnetic resonance spectrum of a radical intermediate in the coenzyme B(12)-dependent ethanolamine ammonia-lyase catalyzed reaction of S-2-aminopropanol.Vahe Bandarian et al.Biochemistry, 41(27), 8580-8588 (2002-07-03) Synthesis of 21-nitrogen substituted pregna-5,17(20)-dienes from pregnenolone.Sergey V Stulov et al.Steroids, 77(1-2), 77-84 (2011-11-09) 5'-Deoxyadenosine contacts the substrate radical intermediate in the active site of ethanolamine ammonia-lyase: 2H and 13C electron nuclear double resonance studies.R LoBrutto et al.Biochemistry, 40(1), 9-14 (2001-01-05) (S)-N-(5-Chlorothiophene-2-sulfonyl)-beta,beta-diethylalaninol a Notch-1-sparing gamma-secretase inhibitor.Derek C Cole et al.Bioorganic & medicinal chemistry letters, 19(3), 926-929 (2008-12-23) An amine: hydroxyacetone aminotransferase from Moraxella lacunata WZ34 for alaninol synthesis.Dongzhi Chen et al.Bioprocess and biosystems engineering, 31(4), 283-289 (2007-09-13)

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