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361346-80-7

361346-80-7 Structure

361346-80-7 Structure
IdentificationBack Directory
[Name]

(1R,2R)-N,N'-BIS(2-ACETYL-3-OXO-2-BUTENYLIDENE)-1,2-DIMESITYLETHYLENEDIAMINATO COBALT(II)
[CAS]

361346-80-7
[Synonyms]

(R)-AMAC
(R,R)-AMAC
(1R,2R)-N,N'-BIS(2-ACETYL-3-OXO-2-BUTENYLIDENE)-1,2-DIMESITYLETHYLENEDIAMINATO COBALT(II)
(E)-3-[[(1R,2R)-2-[[(E)-2-acetyl-3-oxidobut-2-enylidene]amino]-1,2-bis(2,4,6-trimethylphenyl)ethyl]iminomethyl]-4-oxopent-2-en-2-olate
[Molecular Formula]

C32H38CoN2O4
[MDL Number]

MFCD06797061
[MOL File]

361346-80-7.mol
[Molecular Weight]

573.59
Chemical PropertiesBack Directory
[Melting point ]

246-250°C
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[Optical Rotation]

[α]/D 291°, c = 0.1 in chloroform
[InChIKey]

PHCQQLMRNZRDJA-ZQBGJXBSSA-L
[SMILES]

CC(=O)C1=C(C)O[Co]OC(C)=C(\C=N\[C@@H]([C@H](\N=C\1)c2c(C)cc(C)cc2C)c3c(C)cc(C)cc3C)C(C)=O
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H351-H302-H312-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338-P201-P202-P264-P270-P271-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P308+P313-P405-P501
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

22-24/25-36/37/39
[WGK Germany ]

2
[HS Code ]

2942.00.3500
[Storage Class]

13 - Non Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

  • Schiff base-cobalt complex catalyst for asymmetric borohydride reduction of carbonyl compounds

Catalyst for:
  • Enantioselective borohydride reduction
  • Stereoselective preparation of aryl alcohols via asymmetric reduction of aryl ketones with borohydride
  • Stereoselective borohydride reduction of diketones to diols
  • Stereoselective preparation of optically active deuterated primary alcohols via enantioselective borodeuteride reduction of aldehydes
  • Stereoselective preparation of β-hydroxy esters via dynamic kinetic resolution of alkylketo esters with enantioselective borohydride reduction
  • Chemoselective, diastereoselective, and enantioselective borohydride reduction of 1,3-diketones
  • Asymmetric synthesis of diarylhydroxypropanones by stereoselective reduction of alkyldiaryldiketones
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