81937-39-5

Basic information

• Product Name: diethyl 2-(1-(4-acetaMidophenyl)-1-oxopropan-2-yl)Malonate
• Synonyms: diethyl 2-(1-(4-acetaMidophenyl)-1-oxopropan-2-yl)Malonate
• CAS NO: 81937-39-5
• Molecular Formula: C₁₈H₂₃NO₆
• Molecular Weight: 349.37832
• Mol File: 81937-39-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: diethyl 2-(1-(4-acetaMidophenyl)-1-oxopropan-2-yl)Malonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 2-(1-(4-acetaMidophenyl)-1-oxopropan-2-yl)Malonate(81937-39-5)
• EPA Substance Registry System: diethyl 2-(1-(4-acetaMidophenyl)-1-oxopropan-2-yl)Malonate(81937-39-5)

Safety Data

• Hazardous Substances Data: 81937-39-5(Hazardous Substances Data)

Usage

General Description

Diethyl 2-(1-(4-acetamidophenyl)-1-oxopropan-2-yl)malonate is a complex organic chemical compound. As signified by its extensive name, it has a highly specific structural composition. This chemical compound is not widely studied or used and there is not much information available about it like its physical and chemical properties, toxicity, reactivity, stability or potential uses. Its primary recognition comes from being listed in chemical databases. However, based on its structural components, it can be surmised that it could have potential applications in medicinal chemistry, polymer science, pharmaceutical research or similar fields where complex organic compounds are utilized.

Upstream product

• 16960-49-9 N-(4-propionylphenyl)acetamide 
• 103-84-4 Acetanilid 
• 63514-63-6 N-(4-(2-bromopropionyl)phenyl)acetamide 
• 105-53-3 diethyl malonate 
• 81112-08-5 N-[4-(2-chloro-1-oxopropyl)phenyl]acetamide 

Downstream Products

• 1221499-55-3 C₁₈H₁₆N₄O₃ 
• 1221499-56-4 C₁₈H₁₆N₄O₃ 
• 1221499-57-5 C₁₈H₁₇N₃O₃ 
• 1221499-58-6 C₁₈H₁₇N₃O₂ 
• 1221499-59-7 C₁₈H₁₇N₃O₂ 
• 1221499-60-0 C₁₈H₁₆ClN₃O 
• 1221499-61-1 C₂₁H₂₃N₃O₄ 
• 1221499-62-2 C₁₈H₁₅Cl₂N₃O 
• 1221499-63-3 (R)-(-)-6-[4-(2-pyridinylmethylene)amino]phenyl-5-methyl-4,5-dihydro-3(2H)-pyridazinone 
• 1221499-65-5 (R)-(-)-6-[4-(2-furanylmethylene)amino]phenyl-5-methyl-4,5-dihydro-3(2H)-pyridazinone 
• 36725-28-7 OR-1855 
• 136609-85-3 6-(3,4-diaminophenyl)-5-methyl-2,3,4,5-tetrahydropyridazin-3-one 
• 36725-28-7 6-(4-aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone 
• 115344-47-3 2 cyano 1 methyl 3 [4 (4 methyl 6 oxo 1,4,5,6 tetrahydro 3 pyridazinyl)phenyl]guanidine 

Relevant articles and documents

Preparation method of key intermediate of Pimobendan

The invention discloses a preparation method of a key intermediate of Pimobendan. The method comprises steps as follows: (i) a compound I is synthesized; (ii) the compound I is subjected to nucleophilic substitution, and a compound II is produced; (iii) t

Arylalkane, arylalkene and aryl azaalkane, medicaments containing said compounds and method for the production thereof

The present invention relates to compounds of general formula [in-line-formulae]R—Z1—Z2—Z3—R1, ??(I)[/in-line-formulae] wherein R, R1 and Z1 to Z3 are defined as in claim 1, the tautomers, the diastereomers, the enantiomers, the mixtures thereof and the salts thereof, particularly the physiologically acceptable salts thereof with inorganic or organic acids or bases, which have valuable pharmacological properties, particularly CGRP-antagonistic properties, pharmaceutical compositions containing these compounds, their use and processes for preparing them.

6-(substituted phenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-ones of medicinal interest. The synthesis of SK&F 94836 and SK&F 95654

Two synthetic routes to the dihydropyridazinone-cyanoguanidine 4 (SK&F 94836) are described, both proceeding via the anilino compound 6. An efficient synthesis of the dihydropyridazinone-pyridone 5 (SK&F 95654) is reported. This synthesis proceeds via the fluoro-keto-acid 24, with subsequent displacement of the fluoro substituent by 4-pyridone. The surprising effectiveness of water as a solvent in this reaction has been highlighted.