131219-55-1

Basic information

• Product Name: DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT
• Synonyms: DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT;TETRAKIS(N-PHTHALOYL-(S)-PHENYLALANINATO)DIRHODIUM;TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATO]DIRHODIUM ETHYL ACETATE ADDUCT;Tetrakisphthaloylphenylalaninatodirhodium;dirhodium tetrakis[n-phthaloyl-(s)-phenylalaninate];Rh2(S-PTPA)4 EtOAc;Dirhodium Tetrakis[N-phthaloyl-(S)-phenylalaninate] Ethyl Acetate Adduct Rh2(S-PTPA)4 EtOAc;Tetrakis[mu-(2S)-3-phenyl-2-(phthalimido)propanoato]dirhodium
• CAS NO: 131219-55-1
• Molecular Formula: C68H48N4O16Rh2
• Molecular Weight: 1382.94
• Product Categories: Asymmetric Synthesis;Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Metal Complexes;N-Substituted Maleimides, Succinimides & Phthalimides;N-Substituted Phthalimides;Rh (Rhodium) Compounds;Synthetic Organic Chemistry;Transition Metal Compounds
• Mol File: 131219-55-1.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT(CAS DataBase Reference)
• NIST Chemistry Reference: DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT(131219-55-1)
• EPA Substance Registry System: DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT(131219-55-1)

Safety Data

• Hazardous Substances Data: 131219-55-1(Hazardous Substances Data)

Usage

Description

DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT, with the CAS number 131219-55-1, is an organometallic compound that serves as a catalyst in various chemical reactions. It is characterized by its ability to facilitate B-H bond insertion reactions of unstabilized diazo compounds, which are derived from tosylhydrazones. Additionally, it plays a crucial role in the stereoselective preparation of cyclopentane-fused indolines, a type of organic compound with potential applications in pharmaceuticals and materials science.

Uses

Used in Chemical Synthesis:
DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT is used as a catalyst for B-H bond insertion reactions of unstabilized diazo compounds generated from tosylhydrazones. This application is significant because it allows for the efficient formation of new carbon-boron bonds, which are essential in the synthesis of various organic molecules and materials.
Used in Stereoselective Preparation:
DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT is used as a catalyst for the stereoselective preparation of cyclopentane-fused indolines. This application is important in the field of pharmaceuticals and materials science, as it enables the synthesis of specific enantiomers or diastereomers with high selectivity, leading to improved properties and performance of the final products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT is used as a catalyst for the synthesis of complex organic molecules with potential therapeutic applications. Its ability to facilitate B-H bond insertion reactions and stereoselective preparation of cyclopentane-fused indolines makes it a valuable tool in the development of new drugs and drug candidates.
Used in Materials Science:
In the field of materials science, DIRHODIUM TETRAKIS[N-PHTHALOYL-(S)-PHENYLALANINATE] ETHYL ACETATE ADDUCT is used as a catalyst for the synthesis of novel organic compounds with unique properties. These compounds can be used in the development of advanced materials with applications in various industries, such as electronics, aerospace, and automotive.

InChI:InChI=1/4C17H13NO4.C4H8O2.2Rh/c4*19-15-12-8-4-5-9-13(12)16(20)18(15)14(17(21)22)10-11-6-2-1-3-7-11;1-3-6-4(2)5;;/h4*1-9,14H,10H2,(H,21,22);3H2,1-2H3;;/q;;;;;2*+2/p-4/t4*14-;;;/m0000.../s1/r4C17H13NO4.C4H8O2.Rh2/c4*19-15-12-8-4-5-9-13(12)16(20)18(15)14(17(21)22)10-11-6-2-1-3-7-11;1-3-6-4(2)5;1-2/h4*1-9,14H,10H2,(H,21,22);3H2,1-2H3;/q;;;;;+4/p-4/t4*14-;;/m0000../s1