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529486-26-8

529486-26-8 Structure

529486-26-8 Structure
IdentificationBack Directory
[Name]

(2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide
[CAS]

529486-26-8
[Synonyms]

(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrol
(S)-N-((1S,2S)-2-Hydroxy-1,2-diphenylethyl)pyrrolidine-2-carboxamide
(2S)-N-[(1S,2S)-2-hydroxy-1,2-diphenylethyl]pyrrolidine-2-carboxamide
(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxamide
N-[(1S,2S)-2- hydroxy-1,2-diphenylethyl]-(2S)-2-Pyrrolidinecarboxamide
2-Pyrrolidinecarboxamide, N-[(1S,2S)-2-hydroxy-1,2-diphenylethyl]-, (2S)-
(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2- pyrrolidinecarboxamide,99%e.e.
(2S,1μS, 2μS)-Pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenyl-ethyl)amide
(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxaMide >=99% (HPLC)
[Molecular Formula]

C19H22N2O2
[MDL Number]

MFCD10000880
[MOL File]

529486-26-8.mol
[Molecular Weight]

310.39
Chemical PropertiesBack Directory
[Melting point ]

127-131 °C
[storage temp. ]

2-8°C
[Optical Rotation]

[α]/D -25±2°, c = 2 in ethanol
[InChI]

1S/C19H22N2O2/c22-18(15-10-5-2-6-11-15)17(14-8-3-1-4-9-14)21-19(23)16-12-7-13-20-16/h1-6,8-11,16-18,20,22H,7,12-13H2,(H,21,23)/t16-,17-,18-/m0/s1
[InChIKey]

JVOUIFUIIPEWLM-BZSNNMDCSA-N
[SMILES]

O[C@H]([C@@H](NC(=O)[C@@H]1CCCN1)c2ccccc2)c3ccccc3
Safety DataBack Directory
[Hazard Codes ]

T,N
[Risk Statements ]

23/25-50
[Safety Statements ]

45-61
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Aquatic Acute 1
Aquatic Chronic 1
Hazard InformationBack Directory
[Uses]

(2S)-N-[(1S,2S)-2-Hydroxy-1,2-diphenylethyl]-2-pyrrolidinecarboxamide can be used as a catalyst:
  • In the synthesis of α-hydroxyamino?carbonyl compounds by reacting?aldehydes?with?nitrosobenzenes via N-nitroso aldol reaction.
  • In the direct aldol reactions of aldehydes with chloroacetones, methylthio- and fluoroacetones.

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