(S,S)-(+)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) chloride

ALDRICH/404454

Synonym: (S,S)-Jacobsen’s catalyst

CAS Number: 135620-04-1
Empirical Formula (Hill Notation): C₃₆H₅₂ClMnN₂O₂
Molecular Weight: 635.20
MDL Number: MFCD02101663
Linear Formula: [[[(CH₃)₃C]₂C₆H₂-2-(O-)CH=N]₂C₆H₁₀]MnCl
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-404454-1G	1 g	$62.90 1/EA	Add To Favorites
45-404454-5G	5 g	$206.00 1/EA	Add To Favorites
45-404454-25G	25 g	$727.00 1/EA	Add To Favorites

This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 404454-25G

Properties
Descriptions
Safety Info.
Basic Data

InChI	1S/C36H54N2O2.ClH.Mn/c1-33(2,3)25-17-23(31(39)27(19-25)35(7,8)9)21-37-29-15-13-14-16-30(29)38-22-24-18-26(34(4,5)6)20-28(32(24)40)36(10,11)12;;/h17-22,29-30,39-40H,13-16H2,1-12H3;1H;/q;;+3/p-3/b37-21+,38-22+;;/t29-,30-;;/m0../s1
InChI key	LJVAWOSDJSQANR-RUIQGICGSA-K
mp	330-332 °C (lit.)
Quality Level	200
SMILES string	CC(C)(C)c1cc2C=[N@@H]3[C@H]4CCCC[C@@H]4[N@H]5=Cc6cc(cc(c6O[Mn]35(Cl)Oc2c(c1)C(C)(C)C)C(C)(C)C)C(C)(C)C

Application:	Reactant involved in: • Studies of intercalative binding with ct-DNA and radical scavenging antioxidant activity • Immobilization on phenoxy-modified zirconium poly(styrenephenylvinylphosphonate) • Synthesis of derivatvies for studies of conformational models of enantioselective reactions Catalyst involved in: • Asymmetric epoxidation of olefins • Immobilization on ionic liquid modified mesoporous silica for oxidative kinetic resolution of racemic secondary alcohols† • Immobilization on diamine modified zirconium olig-styrenyl phosphonate hydrogen phosphate for epoxidation of styrene
Application:	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. Jacobsen′s catalyst has also been used in the asymmetric α-hydroxylation of silyl enol ethers. Catalyst for the enantioselective epoxidation of a variety of olefins.
General description:	(S,S)-(+)-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.
Legal Information:	Manufactured under license by Sterling Pharma Solutions Limited, using Jacobsen HKR technology.
Packaging:	1, 5, 25 g in glass bottle

Symbol	GHS07
Signal word	Warning
Hazard statements	H315 - H319 - H335
Precautionary statements	P302 + P352 - P305 + P351 + P338
Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

mp	330-332 °C (lit.)
UNSPSC	12352101

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