ChemicalBook Product Catalog Biochemical Engineering Amino Acids and Derivatives Amino alcohol derivative (S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL

(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL

(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Basic information
Product Name:(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
Synonyms:(1S)-1-phenyl-2-[(phenylmethyl)amino]ethanol;(S)-2-Benzylamino-1-phenylethanol,99%e.e.;(S)-(+)-2-Benzylamino-1-phenylethanol;(S)-(+)-2-BenzyL;amino-1-phenyL;Benzenemethanol, α-[[(phenylmethyl)amino]methyl]-, (αS)-;(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL USP/EP/BP;Benzenemethanol, α-[[(phenylmethyl)amino]methyl]-, (αS)-
CAS:51096-49-2
MF:C15H17NO
MW:227.3
EINECS:
Product Categories:Amino Alcohols;Chiral Building Blocks;Organic Building Blocks
Mol File:51096-49-2.mol
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Structure
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Chemical Properties
Melting point 115-118 °C(lit.)
alpha 57 º (C=1 IN CHLOROFORM)
Boiling point 375.2±12.0 °C(Predicted)
density 1.100±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka13.78±0.20(Predicted)
optical activity[α]20/D +57°, c = 1 in chloroform
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29062990
MSDS Information
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Usage And Synthesis
Chemical PropertiesWhite powder
Uses(S)-(+)-2-Benzylamino-1-phenylethanol can be used as an intermediate in the synthesis of aziridines using α-amino and α-amido ketones via asymmetric transfer?hydrogenation?reaction.
General Description(S)-2-Benzylamino-1-phenylethanol can be used as a starting material in the preparation of iron catalysts applicable in the oxidation of secondary alcohols and benzylic methylene groups.
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Preparation Products And Raw materials
Preparation Products(S)-(-)-2-Phenylglycinol
N-(3-CHLOROBENZYL)-2-HYDROXY-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE 2-[(4-CHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL 1,1-BIS(4-CHLOROPHENYL)-2-[(4-FLUOROBENZYL)AMINO]-1-ETHANOL 2-[(4-CHLOROBENZYL)AMINO]-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL 1,1-BIS(4-CHLOROPHENYL)-2-[(2-FLUOROBENZYL)AMINO]-1-ETHANOL 2,2-BIS(4-CHLOROPHENYL)-2-HYDROXY-N-[3-(TRIFLUOROMETHYL)BENZYL]-1-ETHANAMINIUM CHLORIDE 2-[(2,4-DICHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL 1,1-BIS(4-CHLOROPHENYL)-2-[(3-METHOXYBENZYL)AMINO]-1-ETHANOL 1,1-BIS(4-CHLOROPHENYL)-2-[(4-METHOXYBENZYL)AMINO]-1-ETHANOL 2-[(3,4-DICHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL 2-[(3,4-DIMETHOXYBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL 2-HYDROXY-N-(3-METHOXYBENZYL)-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE 2-(BENZYLAMINO)-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL 2-[(3-CHLOROBENZYL)AMINO]-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL 2-[(4-METHOXYBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL 1,1-BIS(4-CHLOROPHENYL)-2-[(4-METHYLBENZYL)AMINO]-1-ETHANOL 2-HYDROXY-N-(2-METHOXYBENZYL)-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE N-(2-CHLOROBENZYL)-2-HYDROXY-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE
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