6186-89-6

Basic information

• Product Name: ethyl methyl propanedioate
• Synonyms: 1-Ethyl 3-methyl malonate
• CAS NO: 6186-89-6
• Molecular Formula: C₆H₁₀O₄
• Molecular Weight: 146.1412
• Mol File: 6186-89-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 190.3°C at 760 mmHg
• Flash Point: 88.4°C
• Density: 1.086g/cm³
• Vapor Pressure: 0.545mmHg at 25°C
• Refractive Index: 1.41
• CAS DataBase Reference: ethyl methyl propanedioate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl methyl propanedioate(6186-89-6)
• EPA Substance Registry System: ethyl methyl propanedioate(6186-89-6)

Safety Data

• Hazardous Substances Data: 6186-89-6(Hazardous Substances Data)

Usage

General Description

Ethyl methyl propanedioate is a chemical compound with the molecular formula C8H14O4. It is derived from the esterification of ethyl alcohol and methyl propanedioic acid. Ethyl methyl propanedioate is commonly used as a flavoring agent and fragrance ingredient in various products such as perfumes, soaps, and cosmetics. It has a fruity, floral odor and is often described as having a sweet, berry-like aroma. ethyl methyl propanedioate is also used in the production of artificial flavorings and as a solvent in various industrial processes. It is important to handle ethyl methyl propanedioate with care, as it can be harmful if ingested or inhaled in large quantities.

Upstream product

• 67-56-1 methanol 
• 627-93-0 hexanedioic acid dimethyl ester 
• 105-53-3 diethyl malonate 
• 6626-84-2 dimethyl 2-benzylidenepropanedioate 
• 105-56-6 ethyl 2-cyanoacetate 
• 1010117-23-3 diethyl 2-nitro-3-oxopentanedioate 
• 64-17-5 ethanol 
• 687-00-3 methyl 4,4,4-trichloroacetoacetate 

Downstream Products

• 113386-82-6 2-(4-Methoxy-phenylthiocarbamoyl)-malonic acid ethyl ester methyl ester 
• 59081-26-4 6-methoxy-2-phenylpyrimidin-4-ol 
• 1253791-97-7 C₁₇H₁₅N₃O₄S 
• 1405680-10-5 (±)-1-ethyl 3-methyl 2-(3-oxo-1-phenyl-3-(phenylamino)propyl)malonate 
• 1405679-71-1 (±)-1-ethyl 3-methyl 2-(3-(hydroxyimino)-1,3-diphenylpropyl)malonate 
• 1405679-90-4 (±)-1-ethyl 3-methyl 2-(3-(tosyloxyimino)butyl)malonate 
• 1405679-56-2 (±)-1-ethyl 3-methyl 2-(3-oxo-1,3-diphenylpropyl)malonate 
• 36600-71-2 ethyl 2-acetyl-3-[4-(1,1-dimethylethyl)phenyl]propanoate 
• 36600-75-6 2-(4-methoxy-benzyl)-3-oxo-butyric acid ethyl ester 
• 14305-31-8 α-acetyl-4-methylbenzenepropanoic acid ethyl ester 
• 1002717-68-1 benzyl-malonic acid ethyl ester methyl ester 
• 24317-95-1 ethyl 2-octylacetoacetate 
• 95314-60-6 1-(ethoxycarbonyl)-1-(p-bromobenzyl)-2-propanone 
• 63218-45-1 ethyl 2-(2,4-dichlorobenzyl)acetoacetate 

Relevant articles and documents

One-by-one hydrogenation, cross-coupling reaction, and Knoevenagel condensations catalyzed by PdCl2 and the downstream palladium residue

A novel catalyst-economic strategy with a recovered palladium catalyst was successfully applied for multi-task and maximum reuse in different types of one-by-one downstream reactions, from catalytic hydrogenation to Suzuki and Sonogashira-type cross-coupling reactions, Knoevenagel condensations, and trans-Knoevenagel-like condensations.

Synthesis of 2/6-(polychloromethyl)pyridinecarboxylates

Due to their relationship to certain bio-active 2,6-(polyfluoromethyl)-3,5-pyridinedicarboxylates 12, methodology was developed to prepare new, but analogous 2/6 (polychloromethyl)pyridinecarboxylates 6, 9, 10, 13, 18 and 20.Successful methods to prepare these materials include several chlorination procedures, mixed Hantzsch sequences, and aluminium chloride interchanges with 12 and 16.

ADDITION OF MALONIC ESTER TO ACRYLIC COMPOUNDS INITIATED BY COORDINATION INITIATORS BASED ON IRON PENTACARBONYL

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