1016985-24-2

1016985-24-2 - Names and Identifiers

Name	(RP)-1-Dicyclohexylphosphino-2-[(R)-alpha-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene
Synonyms	Taniaphos Ligand SL-T002-1 (RP)-1-Dicyclohexylphosphino-2-[(R)-α-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene (RP)-1-Dicyclohexylphosphino-2-[(R)-alpha-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene (R)-(+)-[(R)-2-Dicyclohexylphosphinoferrocenyl](N,N-diMethylaMino)(2-dicyclohexylphosphinophenyl)Methane (R)-1-Dicyclohexylphosphino-2-[(R)-a-(N,N-dimethylamino)-o-(dicyclohexylphosphinophenyl)-methyl]-ferrocene
CAS	1016985-24-2

1016985-24-2 - Physico-chemical Properties

Molecular Formula	C43H63FeNP2
Molar Mass	711.759542
Storage Condition	Room Temprature

1016985-24-2 - Risk and Safety

WGK Germany	3
HS Code	29319090

1016985-24-2 - Introduction

The (RP)-[(R)-alpha-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene is a chiral molecule with the formula C40H54FeN2P2. The following is a detailed description of its nature, use, formulation and safety information:

Nature:
-Appearance: Deep red crystal
-Melting Point: 88-89°C
-Molecular weight: 634.8g/mol
-Stability: stable under dry and anaerobic conditions, but can be decomposed into toxic gases
-Solubility: It is soluble in some organic solvents, such as dichloromethane and tetrahydrofuran

Use:
-As a catalyst: It can be used as a chiral catalyst and act as a catalyst in a variety of organic synthesis reactions. For example, in an asymmetric hydrogenation reaction, it can catalyze an asymmetric hydrogenation reaction to produce a chiral product.

Preparation Method:
-Its synthesis can be obtained by reacting dicyclohexylphosphinoboric acid with the corresponding dicyclohexylphosphinobenzylamine compound. Specific synthetic methods can refer to the relevant scientific literature or patents.

Safety Information:
- (RP)-[(R)-alpha-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene is a toxic compound with potential risks to humans and the environment. When handling and storing the compound, strict safe operating procedures must be followed, and personal protective equipment such as laboratory gloves, goggles and laboratory coats must be used.
-Avoid skin contact and inhalation, and operate in a well-ventilated place if necessary. If contact occurs, rinse immediately with plenty of water and seek medical attention.

Last Update：2024-04-10 22:29:15