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CS-W001157 4
Total: USD 88.00

(R,R)-(-)-N,N'-Bis(3,5-di-tertbutylsalicylidene)-1,2- cyclohexanediaminomanganese(III) chloride

  • CAS No. 138124-32-0

  • Cat. No. CS-W020751
  • Purity≥97%
  • MDL No.MFCD02101664

*For research and further manufacturing use only, not for direct human use.

(R,R)-(-)-N,N'-Bis(3,5-di-tertbutylsalicylidene)-1,2- cyclohexanediaminomanganese(III) chloride|CS-W020751

Structure of 138124-32-0

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General Information

  • CAS No. 138124-32-0
  • Cat. No. CS-W020751
  • Purity ≥97%
  • MDL No. MFCD02101664
  • Storage 4°C, protect from light, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₆H₅₂ClMnN₂O₂
  • Molecular Weight 635.20
  • Synonym(s) (R,R)-Jacobsen's catalyst
  • SMILES Cl[Mn]123[N]([C@H]4[C@H]([N]2=CC5=C(C(C(C)(C)C)=CC(C(C)(C)C)=C5)O3)CCCC4)=CC(C=C(C(C)(C)C)C=C6C(C)(C)C)=C6O1

Description

(R,R)-(-)-N,N-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride is a metal-salen complex that can catalyze a variety of asymmetric transformations(R,R)-()-N,N-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride is a catalyst used in the epoxidation of arenes.Salen (Mn)-catalyzed asymmetric epoxidation of unfunctionalized olefins. High enantioselectivities and yields are obtained for a variety of substrates, especially cis-alkenes. A few applications include the synthesis of the taxol side chain and cis-1-amino-2-indanol. Jacobsens catalyst has also been used in the asymmetric -hydroxylation of silyl enol ethers. Catalyst for the enantioselective epoxidation of a variety of olefins.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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