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Home > Encyclopedia > (-)-(S,S)-1,2-Diphenylethylenediamine

(-)-(S,S)-1,2-Diphenylethylenediamine

(-)-(S,S)-1,2-Diphenylethylenediamine structure

(-)-(S,S)-1,2-Diphenylethylenediamine 

structure
  • CAS No:

    29841-69-8

  • Formula:

    C14H16N2

  • Chemical Name:

    (-)-(S,S)-1,2-Diphenylethylenediamine

  • Synonyms:

    1,2-Ethanediamine,1,2-diphenyl-,(1S,2S)-;Ethylenediamine,1,2-diphenyl-,(1S,2S)-(-)-;1,2-Ethanediamine,1,2-diphenyl-,[S-(R*,R*)]-;(1S,2S)-1,2-Diphenyl-1,2-ethanediamine;(-)-Stilbenediamine;(S,S)-1,2-Diphenylethylenediamine;(S,S)-Stilbenediamine;(S,S)-1,2-Diphenyl-1,2-ethanediamine;(1S,2S)-Diphenyl-1,2-diaminoethane;(-)-1,2-Diphenylethylenediamine;(S,S)-(-)-1,2-Diphenylethylenediamine;(1S,2S)-(-)-1,2-Diphenylethylenediamine;(1S,2S)-1,2-Diphenyl-1,2-diaminoethane;(1S,2S)-1,2-Diphenylethylenediamine;(S,S)-1,2-Diamino-1,2-diphenylethane;(1S,2S)-Diphenylethanediamine;(S,S)-1,2-Diphenyl-1,2-diaminoethane;1,2-(S,S)-Diamino-1,2-diphenylethane;(-)-(S,S)-1,2-Diphenylethylenediamine;(1S,2S)-(-)-1,2-Diphenylethylenediamine;((1S,2S)-2-Amino-1,2-diphenylethyl)amine;(S,S)-1,2-Diphenylethylene-1,2-diamine;(1S,2S)-1,2-Diamino-1,2-diphenylethane;(1S,2S)-1,2-Diphenylethan-1,2-diamine

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

white to light yellow crystal powder

(-)-(S,S)-1,2-Diphenylethylenediamine Basic Attributes

212.29

212.29

3201645

-0

29213000

Characteristics

52

1.4

white to pale yellow crystal

1.1±0.1 g/cm3

82-84 °C

353.9°C at 760 mmHg

199.9±26.0 °C

1.620

Insoluble in water.

2-8°C

3.48E-05mmHg at 25°C

-104 º (c=1.1, MeOH 25 ºC)

Safety Information

8

NONH for all modes of transport

3

36/37/38-34

26-36-45-36/37/39

Xi,C

P261-P305 + P351 + P338

H315-H319-H335

(-)-(S,S)-1,2-Diphenylethylenediamine Use and Manufacturing

Widely used in asymmetric synthesis and optical resolution, such as asymmetric hydroxylation of olefin, asymmetric aldol condensation reaction, asymmetric Diels-Alder reaction, asymmetric allylation of carbonyl group, optically active propadiene Synthesis of alcohols and propynyl alcohols, asymmetric epoxidation of olefins without functional groups and resolution of binaphthol, etc.

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