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Home/Compounds/Research Reagent/(S,S)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminoaluminum chloride
C36H54AlCl3N2O2
680.2 g/mol
Research Reagent

Aluminum, chloro[[2,2'-[(1S,2S)-1,2-cyclohexanediylbis[(nitrilo-kappaN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-kappaO]](2-)]-, (SP-5-13)-

CAS307926-51-8
Category
Research Reagent
Compound Class
Organometallic
Primary Use
Research Compound

This compound is a chiral aluminum complex used as a catalyst in asymmetric synthesis. Its structure features a salen-type ligand coordinated to aluminum, which enables enantioselective transformations in organic chemistry.

Asymmetric synthesis catalystLaboratory research reagent

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Referencestereoisomer of

(T-4)-[[2,2'-[(1R,2R)-1,2-Cyclohexanediylbis[(nitrilo-|EN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-|EO]](2-)]zinc

CAS351498-19-6

research compound

Referencestereoisomer of

(T-4)-[[2,2'-[(1S,2S)-1,2-Cyclohexanediylbis[(nitrilo-|EN)methylidyne]]bis[4,6-bis(1,1-dimethylethyl)phenolato-|EO]](2-)]zinc

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Identifiers
IUPAC Name

aluminum;2,4-ditert-butyl-6-[[(1S,2S)-2-[(3,5-ditert-butyl-2-hydroxyphenyl)methylideneamino]cyclohexyl]iminomethyl]phenol;trichloride

InChIKey

LLAWSRITXLDNBP-FTKQXCDWSA-K

SMILES

CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)O)C=N[C@H]2CCCC[C@@H]2N=CC3=C(C(=CC(=C3)C(C)(C)C)C(C)(C)C)O.[Al+3].[Cl-].[Cl-].[Cl-]

Synonyms (3)

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