Voriconazole Impurity 50

Name: Voriconazole Impurity 50 | 79-03-8
Brand: US-CATO
SKU: S57C4X-136650_25_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C4X-136650_25_MG

Vendor: US-CATO

Product Information

Product Name

Voriconazole Impurity 50

Brand Name

US-CATO

Product Number

C4X-136650

CAS

79-03-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

62324

IUPAC Name

propanoyl chloride

InChI Key

RZWZRACFZGVKFM-UHFFFAOYSA-N

SMILES

CCC(=O)Cl

References Data Source From Pubchem

[11C]Fentanyl: radiosynthesis and preclinical pet imaging for its pharmacokinetics

Publication Name: EJNMMI Radiopharmacy and Chemistry

Publication Date: 2025-10-28

DOI: 10.1186/s41181-025-00394-z

Removal and Recovery Through Chelate Ligand Modified Nanoparticles – A Case for Thiosemicarbazones

Publication Name: Chemistry Africa

Publication Date: 2025-09-23

DOI: 10.1007/s42250-025-01454-2

Design and synthesis of novel indolinone Aurora B kinase inhibitors based on fragment-based drug discovery (FBDD)

Publication Name: Molecular Diversity

Publication Date: 2025-09-10

DOI: 10.1007/s11030-025-11353-w

A Photolabile Backbone Amide Linker for the Solid-Phase Synthesis of Cyclic Peptides and C-terminal Thioesters

Publication Name: International Journal of Peptide Research and Therapeutics

Publication Date: 2025-09-08

DOI: 10.1007/s10989-025-10752-9

Synthesis, Antimicrobial, Anti-Inflammatory, Antioxidant Activities, Molecular Docking, and Dynamic Simulations with Lanosterol 14α-Demethylase of Propionyl Glucopyranoside Derivatives

Publication Name: Russian Journal of Bioorganic Chemistry

Publication Date: 2025-07-28

DOI: 10.1134/s1068162024606554

Voriconazole Impurity 50

Product Information

General Information

References Data Source From Pubchem

[11C]Fentanyl: radiosynthesis and preclinical pet imaging for its pharmacokinetics

Removal and Recovery Through Chelate Ligand Modified Nanoparticles – A Case for Thiosemicarbazones

Design and synthesis of novel indolinone Aurora B kinase inhibitors based on fragment-based drug discovery (FBDD)

A Photolabile Backbone Amide Linker for the Solid-Phase Synthesis of Cyclic Peptides and C-terminal Thioesters

Synthesis, Antimicrobial, Anti-Inflammatory, Antioxidant Activities, Molecular Docking, and Dynamic Simulations with Lanosterol 14α-Demethylase of Propionyl Glucopyranoside Derivatives