N-Methoxy-N-methylacetamide

Name: N-Methoxy-N-methylacetamide | 78191-00-1
Brand: US-CATO
SKU: S57C3D-5545_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57C3D-5545_10_MG

Vendor: US-CATO

Product Information

Product Name

N-Methoxy-N-methylacetamide

Brand Name

US-CATO

Product Number

C3D-5545

CAS

78191-00-1

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

537505

IUPAC Name

N-methoxy-N-methylacetamide

InChI Key

OYVXVLSZQHSNDK-UHFFFAOYSA-N

SMILES

CC(=O)N(C)OC

References Data Source From Pubchem

Combination of bacteriophage–probiotics alleviates intestinal barrier dysfunction by regulating gut microbiome in a chick model of multidrug-resistant Salmonella infection

Publication Name: Journal of Animal Science and Biotechnology

Publication Date: 2026-01-23

DOI: 10.1186/s40104-025-01324-4

Design and synthesis of novel factor XIa Inhibitors with bicyclic isoquinoline and naphthalene fragments

Publication Name: Medicinal Chemistry Research

Publication Date: 2024-05-30

DOI: 10.1007/s00044-024-03245-9

Bromine– or Chlorine–Magnesium Exchange of Aryl Halides in Toluene

Publication Name: Science of Synthesis

Publication Date: 2024

Synthesis of (±)-Myrioneurinol

Publication Name: Synfacts

Publication Date: 2022-05-17

DOI: 10.1055/s-0041-1738193

Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations

Publication Name: Synthesis

Publication Date: 2022-01-04

DOI: 10.1055/a-1684-2942

N-Methoxy-N-methylacetamide

Product Information

General Information

References Data Source From Pubchem

Combination of bacteriophage–probiotics alleviates intestinal barrier dysfunction by regulating gut microbiome in a chick model of multidrug-resistant Salmonella infection

Design and synthesis of novel factor XIa Inhibitors with bicyclic isoquinoline and naphthalene fragments

Bromine– or Chlorine–Magnesium Exchange of Aryl Halides in Toluene

Synthesis of (±)-Myrioneurinol

Enantioselective Syntheses of Yohimbine Alkaloids: Proving Grounds for New Catalytic Transformations