141804-57-1

Basic information

• Product Name: 1,4-Diazabicyclo[2.2.2]octane, 2,5-bis(phenylmethyl)-, (1R,2S,4R,5S)-
• CAS NO: 141804-57-1
• Molecular Formula: C20H24N2
• Molecular Weight: 292.424
• Mol File: 141804-57-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,4-Diazabicyclo[2.2.2]octane, 2,5-bis(phenylmethyl)-, (1R,2S,4R,5S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Diazabicyclo[2.2.2]octane, 2,5-bis(phenylmethyl)-, (1R,2S,4R,5S)-(141804-57-1)
• EPA Substance Registry System: 1,4-Diazabicyclo[2.2.2]octane, 2,5-bis(phenylmethyl)-, (1R,2S,4R,5S)-(141804-57-1)

Safety Data

• Hazardous Substances Data: 141804-57-1(Hazardous Substances Data)

Usage

Chiral Ligand

Used in asymmetric synthesis reactions.
A molecule that can induce a chiral environment in a chemical reaction, leading to the formation of enantiomerically pure compounds.

Enantiomerically Pure Compounds

Creation of enantiomerically pure compounds.
Compounds that consist of only one enantiomer, which are non-superimposable mirror images of each other.

Catalytic Ability

Known for catalyzing a variety of reactions.
The compound can increase the rate of chemical reactions without being consumed in the process.

Carbon-Carbon and Carbon-Heteroatom Bonds

Formation of these bonds.
The compound can facilitate the formation of bonds between carbon atoms and between carbon and other heteroatoms (e.g., nitrogen, oxygen, sulfur).

Pharmaceutical and Medicinal Chemistry

Potential applications in these fields.
The compound's high efficiency in promoting stereoselective reactions makes it valuable for the development of pharmaceuticals and medicines.

Stereoselective Reactions

High efficiency in promoting these reactions.
The compound can selectively produce one enantiomer over another in a chemical reaction, which is crucial for the development of effective drugs with minimal side effects.

Organic Chemistry

Significant interest in the field of organic chemistry.
The compound's unique properties and applications make it an important subject of study in organic chemistry.

Laboratory Research and Industrial Processes

Widely utilized in both settings.
The compound is commonly used in research laboratories for studying its properties and applications, as well as in industrial processes for the production of enantiomerically pure compounds.

Upstream product

• 2862-51-3 (3S,6S)-3,6-dibenzylpiperazine-2,5-dione 
• 13122-89-9 (S)-methyl 2-((S)-2-(tert-butoxycarbonylamino)-3-phenylpropanamido)-3-phenylpropanoate 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 79982-83-5 (2S,5S)-2,5-bis(phenylmethyl)piperazine 
• 106-93-4 ethylene dibromide 
• 141804-54-8 (2S,5S)-2,5-Dibenzyl-4-methoxycarbonylmethyl-piperazine-1-carboxylic acid tert-butyl ester 
• 141804-53-7 (2S,5S)-2,5-Dibenzyl-piperazine-1-carboxylic acid tert-butyl ester 
• 141804-56-0 (2S,5S)-2,5-Dibenzyl-4-(2-chloro-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 
• 141804-55-9 (2S,5S)-2,5-Dibenzyl-4-(2-hydroxy-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 1609286-83-0 (1R,2S,4R,5S)-2,5-dibenzyl-1-methyl-4-aza-1-azoniabicyclo[2.2.2]octane trifluoromethanesulfonate 
• 1609286-85-2 (1S,2S,4S,5S)-2,5-dibenzyl-1-methyl-4-aza-1-azoniabicyclo[2.2.2]octane trifluoromethanesulfonate 

Relevant articles and documents

CHIRAL FLUORINATING REAGENTS

This invention relates to fluorinating agents and, more particularly, to chiral non-racemic fluorinating agents useful for enantioselective fluorination, as well as to their synthesis and use and other subject matter. The fluorinating agents are based on a substituted 1,4-diazabicyclo[2.2.2]octane (DABCO) skeleton and provide electrophillic fluorine enantioselectively.