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(R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride

CAS 164931-83-3N′-Bis(3Chemical Synthesis

(R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride (CAS 164931-83-3) is a chromium(III) complex with the empirical formula C36H52ClCrN2O2 and a molecular weight of 632.26 g/mol. This compound is recognised for its utility as a chiral catalyst in various organic transformations, facilitating stereoselective synthesis. Its applications span asymmetric Mannich reactions, coupling reactions, and cycloadditions, making it a valuable reagent in advanced chemical synthesis.

Synonyms
N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride
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(R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride (N′-Bis(3) — chemical structure, CAS 164931-83-3; Chemistry, fine chemical supplied by Tech Serve Solutions
Asymmetric SynthesisChemical SynthesisChiral CatalystsLigandsand ReagentsCycloadditionSALENs More...
01 /Applications

Asymmetric Anti-Mannich Reactions

This chromium(III) complex serves as an effective catalyst for asymmetric anti-Mannich reactions, enabling the stereoselective formation of valuable carbon-carbon bonds. Its application is crucial in constructing complex molecular architectures with high enantiomeric purity.

Coupling Reactions

It functions as a catalyst in various coupling reactions, contributing to the synthesis of diverse organic molecules. The stereochemical control offered by this catalyst is essential for creating chiral products.

Ring-Opening and Diels-Alder Reactions

The compound facilitates both ring-opening reactions and Diels-Alder cycloadditions. These transformations are fundamental in organic synthesis for building cyclic and polycyclic structures with controlled stereochemistry.

Allylic C-H Oxidation

This catalyst is employed in the allylic C-H oxidation of terminal alkenes. This specific application allows for the selective functionalization of alkene positions, expanding synthetic possibilities.

02 /Properties
Molecular weight632.26
Empirical formulaC36H52ClCrN2O2
ApplicationCatalyst used for:• Asymmetric anti-Mannich reactions1• Coupling reactions2• Ring-opening and Diels-Alder reactions3• Allylic C-H oxidation of terminal alkenes4
Melting point>350 °C(lit.)
03 /Safety & handling
GHS hazard pictogram: Harmful / irritant (GHS07)
Harmful / irritant
Warning

Hazard statements

  • H302Harmful if swallowed
  • H312Harmful in contact with skin
  • H332Harmful if inhaled

Precautionary statements

  • P280Wear protective gloves, clothing and eye/face protection
Protective equipmentdust mask type N95 (US), Eyeshields, Gloves
Water hazard class (WGK, DE)3
Hazard codes (EU)Xn
Risk statements (R)20/21/22
Safety statements (S)26-36

Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.

04 /Identifiers & registry
CAS number
164931-83-3
MDL number
MFCD02684555
PubChem substance
24877848
05 /Quality & supply

Documentation

Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.

Supply & logistics

Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.

06 /Frequently asked questions

What is (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride used for?

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(R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride is primarily used as a chiral catalyst in various organic synthesis reactions, including asymmetric anti-Mannich reactions, coupling reactions, ring-opening reactions, Diels-Alder reactions, and allylic C-H oxidation of terminal alkenes.

What are the CAS number and formula for this chemical?

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The CAS number is 164931-83-3, and the empirical formula is C36H52ClCrN2O2.

What grade and purity does Tech Serve Solutions supply?

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Tech Serve Solutions supplies this product as a research grade chemical. We do not represent it as USP, BP, EP, or pharmacopoeia grade.

How should this chemical be handled safely?

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This compound is classified as harmful if swallowed, in contact with skin, or if inhaled (H302, H312, H332). Handle with appropriate personal protective equipment, including a dust mask (type N95 US), eyeshields, and gloves. Ensure adequate ventilation.

Is this chemical exported by Tech Serve Solutions?

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Yes, Tech Serve Solutions is a specialist global supplier and exporter of fine chemicals, including (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride.

How can I request a sample or quote?

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To request a sample or a quote for (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride, please contact our sales team through the website or by phone.

Need (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminochromium(III) chloride in a specific grade or volume?