ChemicalBook > CAS DataBase List > (S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
- CAS No.51096-49-2
- Chemical Name:(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL
- CBNumber:CB8499794
- Molecular Formula:C15H17NO
- Formula Weight:227.3
- MOL File:51096-49-2.mol
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Property
- 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
- UNSPSC Code 12352116
- NACRES NA.22
Safety
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H315-H319-H335
- Precautionary statements P261-P264-P271-P280-P302+P352-P305+P351+P338
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Price
More Price(1)
- Brand: Sigma-Aldrich(India)
- Product number: 551996
- Product name : (S)-(+)-2-Benzylamino-1-phenylethanol
- Purity: 97%
- Packaging: 1G
- Price: ₹1818.6
- Updated: 2022/06/14
- Buy: Buy
(S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOL Chemical Properties,Usage,Production
- 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-PHENYLETHANOL Preparation Products And Raw materials
Raw materials
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51096-49-2, (S)-(+)-2-BENZYLAMINO-1-PHENYLETHANOLRelated Search:
- 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
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