Rivastigmine EP Impurity H

Name: Rivastigmine EP Impurity H | 586-37-8
Brand: US-CATO
SKU: S57C4X-13848_10_MG
Price: 19998.0 USD
Availability: InStock

Cat. No S57C4X-13848_10_MG

Vendor: US-CATO

Product Information

Product Name

Rivastigmine EP Impurity H

Brand Name

US-CATO

Product Number

C4X-13848

CAS

586-37-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11460

IUPAC Name

1-(3-methoxyphenyl)ethanone

InChI Key

BAYUSCHCCGXLAY-UHFFFAOYSA-N

SMILES

CC(=O)C1=CC(=CC=C1)OC

References Data Source From Pubchem

High-Efficient Synthesis of Fluorescent Ketazine Derivatives Using Nickel Phosphate Heterogeneous Catalyst

Publication Name: Journal of Fluorescence

Publication Date: 2025-12-06

DOI: 10.1007/s10895-025-04593-4

Copper cobaltate loaded on hollow carbon spheres: enhanced catalytic performance for transfer hydrogenation of acetophenone derivatives

Publication Name: Carbon Letters

Publication Date: 2025-05-27

DOI: 10.1007/s42823-025-00920-8

Design, synthesis, and anti-breast cancer activity evaluation of novel 3-cyanopyridine derivatives as PIM-1 inhibitors

Publication Name: Molecular Diversity

Publication Date: 2024-11-09

DOI: 10.1007/s11030-024-11010-8

Palladium-Catalyzed Cross Coupling of Aryl Bromides with Alkenyllithium Reagents

Publication Name: Science of Synthesis

Publication Date: 2024

A pharmacophore-based approach to demonstrating the scope of alcohol dehydrogenases

Publication Name: Bioorganic & Medicinal Chemistry

Publication Date: 2023-04-01

DOI: 10.1016/j.bmc.2023.117255

Rivastigmine EP Impurity H

Product Information

General Information

References Data Source From Pubchem

High-Efficient Synthesis of Fluorescent Ketazine Derivatives Using Nickel Phosphate Heterogeneous Catalyst

Copper cobaltate loaded on hollow carbon spheres: enhanced catalytic performance for transfer hydrogenation of acetophenone derivatives

Design, synthesis, and anti-breast cancer activity evaluation of novel 3-cyanopyridine derivatives as PIM-1 inhibitors

Palladium-Catalyzed Cross Coupling of Aryl Bromides with Alkenyllithium Reagents

A pharmacophore-based approach to demonstrating the scope of alcohol dehydrogenases