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
- Product Categories:
-
- Amino Alcohols
- Chiral Building Blocks
- Organic Building Blocks
- Mol File:
- 51096-49-2.mol
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(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
- pka
- 13.78±0.20(Predicted)
- optical activity
- [α]20/D +57°, c = 1 in chloroform
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(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Usage And Synthesis
Chemical Properties
White 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-PHENYLETHANOLSupplier
J & K SCIENTIFIC LTD.
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- 010-82848833 400-666-7788
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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ForeChem (Nantong) Technology Co.,Ltd.
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- 513-85982855 18921614129
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Energy Chemical
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Capot Chemical Co., Ltd
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- +86 (0) 571 85 58 67 18
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(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL(51096-49-2)Related Product Information
- 2-[(4-METHYLBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- N-(3-CHLOROBENZYL)-2-HYDROXY-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE
- 2-[(2,4-DICHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- 2-[(3,4-DICHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- 1,1-BIS(4-CHLOROPHENYL)-2-[(4-METHYLBENZYL)AMINO]-1-ETHANOL
- 2-[(3-CHLOROBENZYL)AMINO]-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL
- 2-(BENZYLAMINO)-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL
- 1,1-BIS(4-CHLOROPHENYL)-2-[(4-METHOXYBENZYL)AMINO]-1-ETHANOL
- 1,1-BIS(4-CHLOROPHENYL)-2-[(3-METHOXYBENZYL)AMINO]-1-ETHANOL
- 2-[(4-CHLOROBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- 2,2-BIS(4-CHLOROPHENYL)-2-HYDROXY-N-[3-(TRIFLUOROMETHYL)BENZYL]-1-ETHANAMINIUM CHLORIDE
- 2-[(4-CHLOROBENZYL)AMINO]-1,1-BIS(4-CHLOROPHENYL)-1-ETHANOL
- 1,1-BIS(4-CHLOROPHENYL)-2-[(2-FLUOROBENZYL)AMINO]-1-ETHANOL
- 2-[(4-METHOXYBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- 1,1-BIS(4-CHLOROPHENYL)-2-[(4-FLUOROBENZYL)AMINO]-1-ETHANOL
- 2-[(3,4-DIMETHOXYBENZYL)AMINO]-1,1-DIPHENYL-1-ETHANOL
- N-(2-CHLOROBENZYL)-2-HYDROXY-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE
- 2-HYDROXY-N-(2-METHOXYBENZYL)-2,2-DIPHENYL-1-ETHANAMINIUM CHLORIDE