(S,S)-ET-DUPHOS-RH

(S,S)-ET-DUPHOS-RH - Names and Identifiers

Name	(+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate
Synonyms	(S,S)-ET-DUPHOS-RH (+)-1,2-BIS((2S,5S)-DIETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM(I) TRIFLATE (+)-1,2-BIS(2S,5S)-2,5-(DIETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM(I)TRIFLUOROMETHANSULFONATE (+)-1,2-BIS((2S,5S)-2,5-DIETHYLPHOSPHOLANO)BENZENE(CYCLOOCTADIENE)RHODIUM (I) TRIFLUOROMETHANESULFONATE (+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate (+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodiuM(I) trifluoroMethanesulfonate (S,S)-Et-DUPHOS-Rh
CAS	142184-30-3

(S,S)-ET-DUPHOS-RH - Physico-chemical Properties

Molecular Formula	C31H48F3O3P2RhS
Molar Mass	722.62
Appearance	crystal
Color	orange
Storage Condition	Inert atmosphere,2-8°C
Sensitive	Air & Moisture Sensitive
MDL	MFCD00269861

(S,S)-ET-DUPHOS-RH - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S24/25 - Avoid contact with skin and eyes. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
WGK Germany	3
HS Code	29310099

(S,S)-ET-DUPHOS-RH - Introduction

()-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate is an organic complex with the chemical formula [(C2H5)2C6H3P]2(Rh)C8H12(COD)(CF3SO3). The following is a description of the properties, use, preparation and safety information of the compound:

Nature:
-Appearance: This compound is usually powdery and light yellow in color.
-Solubility: Can be dissolved in some common organic solvents, such as ether, nitrile and dimethylformamide.
-Stability: relatively stable in the air, but avoid exposure to moisture and high temperature conditions.
-Melting point: The compound has a higher melting point.

Use:
-Catalyst: This compound is an important complex catalyst, usually used in organic synthesis reactions such as hydrogenation, hydrogenation, hydrogen transfer, and catalytic olefin reactions.
-Asymmetric synthesis: The chiral ligand structure of this compound makes it particularly suitable for asymmetric synthesis reactions and can be used to synthesize chiral compounds.

Preparation Method:
-The preparation of this compound is generally carried out through a multi-step synthesis process, which requires a series of organic synthesis and coordination chemistry reactions. The specific synthetic method may vary depending on the literature and the research laboratory.

Safety Information:
-The compound is generally relatively safe under correct use and handling, but the following points still need to be paid attention:
-Direct contact with skin, eyes and respiratory tract should be avoided to prevent possible irritation and inhalation.
-Wear appropriate personal protective equipment, such as laboratory gloves, goggles and protective face shields.
-When using or handling this compound, operate according to local chemical handling regulations and follow safe operating procedures.

Please note that the detailed experimental conditions and safety handling details of the compound should be based on specific laboratory and application needs, referring to relevant literature and professional guidelines.

Last Update：2024-04-10 22:29:15