Product Name:(1R,1''R)-3,3''-[[(1S,2S)-Cyclohexane-1,2-diylbis(azanediyl)]bis(methylene)]bis(2'-benzyl-[1,1'-binaphthalen]-2-ol)

IUPAC Name:2'-benzyl-3-({[(1S,2S)-2-[({2'-benzyl-2-hydroxy-[1,1'-binaphthalen]-3-yl}methyl)amino]cyclohexyl]amino}methyl)-[1,1'-binaphthalen]-2-ol

CAS:1403589-08-1
Molecular Formula:C62H54N2O2
Purity:95%
Catalog Number:CM117408
Molecular Weight:859.13

Packing Unit Available Stock Price($) Quantity
CM117408-500mg 1-2 Weeks ƿƛȡ

For R&D use only.

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Product Details

CAS NO:1403589-08-1
Molecular Formula:C62H54N2O2
Melting Point:-
Smiles Code:OC1=C(CN[C@@H]2[C@@H](NCC3=C(O)C(C4=C5C=CC=CC5=CC=C4CC6=CC=CC=C6)=C7C=CC=CC7=C3)CCCC2)C=C8C=CC=CC8=C1C9=C%10C=CC=CC%10=CC=C9CC%11=CC=CC=C%11
Density:
Catalog Number:CM117408
Molecular Weight:859.13
Boiling Point:
MDL No:MFCD30833869
Storage:

Category Infos

Naphthalenes
Naphthalene is a hydrocarbon produced by the distillation of coal tar and is an aromatic white crystalline substance. Naphthalene is the most abundant component in coal tar. It is used as an insect repellant and insect fumigant. The compound is used in the manufacture of celluloid, dyes, hydrogenated naphthalenes, oil fumes, smokeless powders and synthetic resins.
Cyclohexanes
Cyclohexane is an organic compound with a chemical formula C6H12. It is a colorless liquid with a pungent odor, insoluble in water, and soluble in most organic solvents such as ethanol, ether, benzene, and acetone. Cyclohexyl fragments are a common structure in both natural and synthetic drugs. It can be used as both core structure and part of achiral side chain.

Column Infos

Catalysts and Ligands
A catalyst refers to a substance that increases the rate of a reaction without changing the overall standard Gibbs free energy change of the reaction. Ligands represent atoms, molecules, and ions that can bond with a central atom (metal or metalloid). In general, ligands will donate at least one electron when participating in a bond. Two-phase catalysis of catalysts and ligands is the first application in the field of fluorine chemistry. The method of self-fluorine two-phase catalysis has developed rapidly, and a large number of new fluorine-based catalysts and ligands (especially phosphines) have been obtained in the field of chemistry.