442686-32-0

Basic information

• Product Name: (3-BroMo-2,6-diMethoxy-4-pyridyl)di-3,5-xylylphosphine oxide
• Synonyms: (3-BroMo-2,6-diMethoxy-4-pyridyl)di-3,5-xylylphosphine oxide
• CAS NO: 442686-32-0
• Molecular Formula: C₂₃H₂₅BrNO₃P
• Molecular Weight: 474
• Mol File: 442686-32-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 220-222℃
• Boiling Point: 613.7±55.0 °C(Predicted)
• Appearance: /
• Density: 1.36±0.1 g/cm3(Predicted)
• PKA: -3.85±0.36(Predicted)
• CAS DataBase Reference: (3-BroMo-2,6-diMethoxy-4-pyridyl)di-3,5-xylylphosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (3-BroMo-2,6-diMethoxy-4-pyridyl)di-3,5-xylylphosphine oxide(442686-32-0)
• EPA Substance Registry System: (3-BroMo-2,6-diMethoxy-4-pyridyl)di-3,5-xylylphosphine oxide(442686-32-0)

Safety Data

• Hazardous Substances Data: 442686-32-0(Hazardous Substances Data)

Usage

Description

(3-Bromo-2,6-dimethoxy-4-pyridyl)di-3,5-xylylphosphine oxide is a phosphine oxide derivative with the molecular formula C24H26BrNO3P. It features a bromo-pyridine moiety and two xylyl groups, making it a unique chemical compound with potential applications in various fields.

Uses

Used in Organic Synthesis:
(3-Bromo-2,6-dimethoxy-4-pyridyl)di-3,5-xylylphosphine oxide is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile chemical reactions and the formation of a wide range of compounds.
Used as a Ligand in Transition Metal Catalysis:
In the field of transition metal catalysis, (3-Bromo-2,6-dimethoxy-4-pyridyl)di-3,5-xylylphosphine oxide serves as a ligand, enhancing the catalytic activity and selectivity of metal complexes. Its presence can improve the efficiency of various chemical reactions and contribute to the development of new catalytic processes.
Potential Biological Activity:
Although further research is required, (3-Bromo-2,6-dimethoxy-4-pyridyl)di-3,5-xylylphosphine oxide may exhibit biological activity, making it a candidate for pharmaceutical or agrochemical applications. Its unique structure could potentially interact with biological targets, leading to new therapeutic or pesticidal agents.
Note: Since the provided materials do not specify particular industries for the applications, the uses are described in a general context. If specific industries are mentioned in the future, the applications can be tailored accordingly.

Upstream product

• 442686-31-9 4-[bis-(3,5-dimethyl-phenyl)-phosphanyl]-3-bromo-2,6-dimethoxy-pyridine 
• 13445-16-4 3-bromo-2,6-dimethoxypyridine 
• 34696-73-6 3,5-dimethyphenylmagnesium bromide 
• 74289-57-9 bis-(3,5-dimethylphenyl)chlorophosphine 

Downstream Products

• 442905-31-9 4,4'-bis-[bis-(3,5-dimethyl-phenyl)-phosphinoyl]-2,6,2',6'-tetramethoxy-[3,3']bipyridinyl 
• 442905-31-9 4,4'-bis-[bis-(3,5-dimethyl-phenyl)-phosphinoyl]-2,6,2',6'-tetramethoxy-[3,3']bipyridinyl 
• 443347-10-2 (S)-2,2',6,6'-tetramethoxy-4,4'-bis(di(3,5-xylyl)phosphino)-3,3'-bipyridine 
• 442905-33-1 (R)-(+)-2,2',6,6'-tetramethoxy-4,4'-bis(di(3,5-xylyl)phosphino)-3,3'-bipyridine 

Relevant articles and documents

A new chiral dipyridylphosphine ligand Xyl-P-Phos and its application in the Ru-catalyzed asymmetric hydrogenation of β-ketoesters

A new chiral dipyridylphosphine ligand Xyl-P-Phos has been synthesized and the structure of (S)-Xyl-P-Phos oxide has been characterized by single crystal X-ray diffraction. The ruthenium complex of this ligand, Ru(R-Xyl-P-Phos)(C6H6)Cl2, has been found to be a highly active, enantioselective and air-stable catalyst for the asymmetric hydrogenation of β-ketoesters and shows good potential for industrial applications.