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(S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)

Names

[ CAS No. ]:
188264-84-8

[ Name ]:
(S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)

[Synonym ]:
(-)-1,2-bis((2S,5S)-2,5-diisiopropyl phosphorano) benzene
(S,S)-Fmoc-trans-2-aminocyclopentanecarboxylic acid-OH
(S,S)-Jocobsen's catalyst
(1S,2S)-2-(9H-fluoren-9-ylmethoxycarbonyl)amino-cyclopentanecarboxylic acid
Fmoc-(S,S)-2-aminocyclopentanecarboxylic acid
(1S,2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}cyclopentane-1-carboxylic acid
1,2-bis(2,5-diisopropylphospholano)benzene
MFCD01631278
(S,S)-Co-salen complex
Fmoc-(S,S)-ACPC
(S,S)-iPrDuPhos
Cyclopentanecarboxylicacid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-,(1S,2S)
(S,S)-(-)-N-N'-bis(3,5-di-tert-butylsalicylidine)-1,2-cyclohexanediaminocobalt-II
(R,R)-i-Pr-DuPhos
(S,S)-(+)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-COBALT(II)
Jacobsen's (S,S)-(salen)Co(III) catalyst
(S,S)-(salen)Co(II)
2,2'-{(1S,2S)-1,2-Cyclohexanediylbis[nitrilo(E)methylylidene]}bis[4,6-bis(2-methyl-2-propanyl)phenol] - cobalt (1:1)
(S,S)-Co-Salen
(S,S)-Fmoc-trans-2-aminocyclopentanecarboxylic acid
(S,S)-Fmoc-ACPC-OH
Phenol, 2,2'-[(1S,2S)-1,2-cyclohexanediylbis[nitrilo(E)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)-, cobalt salt (1:1)
(S,S)-(+)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)

Chemical & Physical Properties

[ Melting Point ]:
>350ºC(lit.)

[ Molecular Formula ]:
C36H54CoN2O2

[ Molecular Weight ]:
605.759

[ Exact Mass ]:
605.351746

[ PSA ]:
65.18000

[ LogP ]:
9.13700

MSDS

Safety Information

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
36/37/39

[ RIDADR ]:
NONH for all modes of transport

Synthetic Route

Precursor & DownStream

Articles

Asymmetric catalysis with water: efficient kinetic resolution of terminal epoxides by means of catalytic hydrolysis.

Science 277 , 936, (1997)

Epoxides are versatile building blocks for organic synthesis. However, terminal epoxides are arguably the most important subclass of these compounds, and no general and practical method exists for the...

Jacobsen, E.N. et al.

Tetrahedron Lett. 38 , 773, (1997)


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