41378-30-7

Basic information

• Product Name: Pyrrolidine, 1-(2-Methylphenyl)-
• Synonyms: Pyrrolidine, 1-(2-Methylphenyl)-;1-(2-methylphenyl)Pyrrolidine
• CAS NO: 41378-30-7
• Molecular Formula: C₁₁H₁₅N
• Molecular Weight: 161.2435
• Mol File: 41378-30-7.mol
• Article Data: 29

Chemical Properties

• Boiling Point: 255°Cat760mmHg
• Flash Point: 98.8°C
• Appearance: /
• Density: 1.006g/cm³
• Vapor Pressure: 0.0167mmHg at 25°C
• Refractive Index: 1.553
• CAS DataBase Reference: Pyrrolidine, 1-(2-Methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrrolidine, 1-(2-Methylphenyl)-(41378-30-7)
• EPA Substance Registry System: Pyrrolidine, 1-(2-Methylphenyl)-(41378-30-7)

Safety Data

• Hazardous Substances Data: 41378-30-7(Hazardous Substances Data)

Usage

General Description

Pyrrolidine, 1-(2-Methylphenyl)- is a chemical compound with the molecular formula C11H15N. It is a derivative of pyrrolidine and contains a methylphenyl group. Pyrrolidine, 1-(2-Methylphenyl)- is used in various fields, including pharmaceuticals, agrochemicals, and organic synthesis. It is known for its role as a building block in the synthesis of various compounds, and it exhibits biological activity in certain applications. Additionally, it is used as a starting material in the creation of other chemicals and materials. Overall, Pyrrolidine, 1-(2-Methylphenyl)- has several important applications and is a valuable compound in the chemical industry.

InChI:InChI=1/C11H15N/c1-10-6-2-3-7-11(10)12-8-4-5-9-12/h2-3,6-7H,4-5,8-9H2,1H3

Upstream product

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Downstream Products

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Relevant articles and documents

Synthesis of N-heterocyclic carbene-Pd(II)-5-phenyloxazole complexes and initial studies of their catalytic activity toward the Buchwald-Hartwig amination of aryl chlorides

Three new N-heterocyclic carbene (NHC)-Pd(II) complexes using 5-phenyloxazole as the ancillary ligand have been obtained in moderate to good yields by a one-pot reaction of the corresponding imidazolium salts, palladium chloride and 5-phenyloxazole under mild conditions. Initial studies showed that one of the complexes is an efficient catalyst for the Buchwald-Hartwig amination of aryl chlorides with various secondary and primary amines under the varied catalyst loading of 0.01-0.05 mol%, thus it will enrich the chemistry of NHCs and give an alternative catalyst for the coupling of challenging while cost-low aryl chlorides.

Tropane alkaloid compounds and method of manufacturing using sequential oxidation reactions

The present invention relates to a tropane alkaloid compound sequentially using an oxidative Mannich ring reaction and a method for producing the same. The present invention provides a tropane alkaloid compound having a structure of chemical formula 1 in

Aryl-Diadamantyl Phosphine Ligands in Palladium-Catalyzed Cross-Coupling Reactions: Synthesis, Structural Analysis, and Application

Synthesis, temperature-dependent NMR structure investigation and utilization of a new, stable and easily accessible aryl-diadamantylphosphine ligand family is reported. The bulky and electron-rich phosphorus center of the ligand enhances the catalytic activity of palladium in cross-coupling reactions of sterically demanding ortho-substituted aryl halides. In our study, we demonstrated the synthetic applicability of the new phosphine ligands in Buchwald-Hartwig and tosyl hydrazone coupling reactions.