323193-85-7

Basic information

• Product Name: 2,2'-((1R,2R)-1,2-CYCLOHEXANEDIYLBIS((E&
• Synonyms: 2,2μ-[(1R,2R)-(-)-1,2-Cyclohexanediylbis((E)-(nitrilomethylidyne))]bis[4-(tert-butyl)-6-(4-morpholinylmethyl)phenol];N,Nμ-Bis[(E)-5-(tert-butyl)-2-hydroxy-3-(4-morpholinylmethyl)benzylidene]-[(1R,2R)-1,2-cyclohexanediamine]
• CAS NO: 323193-85-7
• Molecular Formula: C38H56N4O4
• Molecular Weight: 632.884
• Mol File: 323193-85-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 132-140 °C
• Boiling Point: 729.1°C at 760 mmHg
• Flash Point: 394.7°C
• Appearance: /
• Density: 1.16g/cm³
• Vapor Pressure: 5.72E-22mmHg at 25°C
• Refractive Index: 1.588
• PKA: 13.05±0.40(Predicted)
• CAS DataBase Reference: 2,2'-((1R,2R)-1,2-CYCLOHEXANEDIYLBIS((E&(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-((1R,2R)-1,2-CYCLOHEXANEDIYLBIS((E&(323193-85-7)
• EPA Substance Registry System: 2,2'-((1R,2R)-1,2-CYCLOHEXANEDIYLBIS((E&(323193-85-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• Hazardous Substances Data: 323193-85-7(Hazardous Substances Data)

Usage

Molecular structure

The compound consists of two cyclohexane rings connected by a central carbon atom, with two ethyl groups attached in an E conformation.

Application in organic chemistry

The unique structure and properties of the compound make it a potential candidate for use in various chemical processes and reactions.

Application in materials science

The compound's structural properties may make it useful in the development of new materials.

Application in pharmaceuticals

The compound may have potential biological activity that could be of interest for medicinal research and drug development.

Need for further research

More research and experimentation are needed to fully understand the potential uses and properties of this chemical.

InChI:InChI=1/C38H56N4O4/c1-37(2,3)31-19-27(35(43)29(21-31)25-41-11-15-45-16-12-41)23-39-33-9-7-8-10-34(33)40-24-28-20-32(38(4,5)6)22-30(36(28)44)26-42-13-17-46-18-14-42/h19-24,33-34,43-44H,7-18,25-26H2,1-6H3/b39-23+,40-24+/t33-,34-/m1/s1

Upstream product

• 98-54-4 para-tert-butylphenol 
• 2725-53-3 2-hydroxy-5-t-butylbenzaldehyde 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 252735-68-5 2-Hydroxy-3-(morpholin-4-ylmethyl)-5-tert-butylbenzaldehyde 
• 23039-28-3 3-(tert-butyl)benzaldehyde 
• 18811-63-7 N-(ethoxymethyl)morpholine 
• 1121-22-8 trans-1,2-Diaminocyclohexane 

Relevant articles and documents

METHOD OF PREPARING POLY(ALKYLENE CARBONATE) VIA COPOLYMERIZATION OF CARBON DIOXIDE/EPOXIDE IN THE PRESENCE OF NOVEL COMPLEX

Provided is a method of preparing poly(alkylene carbonate) using a molecular weight regulator in a process of preparing a copolymer of carbon dioxide/epoxide using a novel complex synthesized from salen-type ligand including a quaternary ammonium salt as a catalyst. According to the present invention, even though the molecular weight regulator is used, an activity of the catalyst may be stably maintained, whereby the low molecular weight of poly(alkylene carbonate) having a desirable level may be effectively provided. In addition, it is expected that since the novel complex as the catalyst of the present invention has a simple structure as compared to the existing copolymerization catalyst, due to the economical preparation cost thereof, the novel complex may be effectively applied to a large-scale commercial process.

Salen-derived catalysts containing secondary basic groups in the addition of diethylzinc to aldehydes

matrix presented A set of modular bifunctional salen catalysts which contain Lewis acid and Lewis base activating groups is described. These groups can be altered independently to control nucleophilic and electrophilic activation of the reacting substrates. These salen-derived catalysts show enhanced reactivity in the addition of diethylzinc to aldehydes with respect to most other salen, amino alcohol, and diamine derived catalysts and reactivity comparable to that of Ti complexes of bis-sulfonamides and diols.