ChemicalBook > Product Catalog > Organic Chemistry > Organometallic compounds > Organic manganese > (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE
(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE
(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE Basic information
- Product Name:
- (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE
- CAS:
- 138124-32-0
- MF:
- C36H52ClMnN2O2
- MW:
- 635.2
- Mol File:
- 138124-32-0.mol
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(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE Chemical Properties
- Melting point:
- 330-332 °C(lit.)
- alpha
- D23 +580° (c = 0.01 in ethanol)
- form
- Liquid May Develop Some Turbidity or Precipitate
- color
- Light yellow to gold to brown
- λmax
- 509nm(CH2Cl2)(lit.)
- Merck
- 14,5252
- InChIKey
- LJVAWOSDJSQANR-OHRASPNLSA-K
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Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-20/21/22
- Safety Statements
- 26-36-36/37/39
- WGK Germany
- 3
- F
- 9
- HS Code
- 29349990
MSDS
- Language:EnglishProvider:SigmaAldrich
- Language:EnglishProvider:ACROS
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(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE Usage And Synthesis
Chemical Properties
(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE is Dark brown powder or chunks
Uses
(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE is a coordinated compound of manganese and a salen-type ligand. It is also used as an asymmetric catalyst used to enantioselectively transform prochiral alkenes into epoxides.
Uses
Chiral catalyst for epoxidation of olefins.
Reactions
- Catalyst for the conversion of olefins to chiral epoxides in high enantiomeric excess.
- Pharmaceutically important, single enantiomer amino alcohols are efficiently produced from the corresponding chiral epoxide by acid or base-catalyzed epoxide ring-opening reactions.
- symmetric Kinetic resolution of secondary alcohols in water.
- Enantioselective Reformatsky reaction with ketones.

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(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE(138124-32-0)Related Product Information
- (S,S)-(+)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE
- (1R,2R)-(-)-[1,2-CYCLOHEXANEDIAMINO-N N'-BIS(3,5-DI-T-BUTYLSALICYLIDENE)]CHROMIUM (III) CHLORIDE
- Manganese
- Manganese chloride tetrahydrate
- (R,R)-(-)-1,2-DIAMINOCYCLOHEXANE HYDROCHLORIDE
- CIS/TRANS-DISALYCYLIDENE-1,2-CYCLOHEXYLIDENEDIAMINE
- N,N'-BIS(SALICYLIDENE)-1,2-PROPANEDIAMINE
- N-benzylidenecyclohexylamine
- N,N'-BIS(SALICYLIDENE)ETHYLENEDIAMINE
- (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINE
- N,N'-BIS(SALICYLIDENE)-1,6-HEXANEDIAMINE
- (R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDE
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(R,R)-(-)-N,N'-BIS(3,5-DI-TERT-BUTYLSALICYLIDENE)-1,2-CYCLOHEXANEDIAMINO-MANGANESE(III) CHLORIDESupplierMore
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