CAS 609-09-6

Diethyl ketomalonate

Description:

Diethyl ketomalonate, with the CAS number 609-09-6, is an organic compound that belongs to the class of ketones and esters. It is characterized by its structure, which features two ethyl ester groups attached to a central ketone moiety. This compound is typically a colorless to pale yellow liquid with a fruity odor. Diethyl ketomalonate is known for its reactivity in various organic synthesis reactions, particularly in the formation of carbon-carbon bonds, making it a valuable intermediate in the synthesis of pharmaceuticals and other complex organic molecules. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. The compound is also recognized for its ability to undergo condensation reactions, which can lead to the formation of larger, more complex molecules. Safety precautions should be taken when handling diethyl ketomalonate, as it may pose health risks if ingested or inhaled, and appropriate personal protective equipment should be used.

Formula: C₇H₁₀O₅

InChI: InChI=1/C7H10O5/c1-3-11-6(9)5(8)7(10)12-4-2/h3-4H2,1-2H3

InChI key: InChIKey=DBKKFIIYQGGHJO-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)(C(OCC)=O)=O

Synonyms:

• 1,3-Diethyl 2-oxopropanedioate
• 2-Oxomalonic acid diethyl ester
• Carbonyl diethyl malonate
• Diethyl 2-oxomalonate
• Diethyl 2-oxopropane-1,3-dioate
• Diethyl Oxopropanedioate
• Diethyl mesoxalate
• Diethyl oxomalonate
• Diethyloxomalonate
• Ethoxycarbonyl ethoxycarbonyl ketone
• Ethyl ketomalonate
• Ethyl mesoxalate
• Ethyl oxomalonate
• Mesoxalic acid, diethyl ester
• NSC 53478
• Oxopropanedioic acid diethyl ester
• Propanedioic acid, 2-oxo-, 1,3-diethyl ester
• Propanedioic acid, oxo-, diethyl ester
• DIETHYL MESOXYLATE
• KETOMALONIC ACID DIETHYL ESTER
• 2-Oxopropanedioic acid diethyl
• Diethyl ketomalonate 97%
• DIETHYL KETOMALONATE
• DiethylKetomaloante
• Diethylmesoxalate=Diethyloxomalonate
• Diethyl ketomalonate, (Diethyl mesoxalate
• Diethyl ketomalonate, Ketomalonic acid diethyl ester
• oxo-propanedioicacidiethylester
• Diethyl mesoxalate, Ketomalonic acid diethyl ester
• Diethyl mesoxalate~Diethyl oxomalonate~Oxopropanedioic acid diethyl ester

Diethyl Mesoxalate

CAS: 609-09-6

Formula: C₇H₁₀O₅

Purity: >94.0%(GC)

Color and Shape: White to Yellow to Green clear liquid

Molecular weight: 174.15

Ref: 3B-M0866

Diethyl ketomalonate, 95%

CAS: 609-09-6

Diethyl ketomalonate, reagent employed in Wittig and Aza-Wittig reactions for synthesis of triazoles, and 2-azadienes, respectively. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legac

Formula: C₇H₁₀O₅

Purity: 95%

Color and Shape: Clear colorless to yellow, Liquid

Molecular weight: 174.15

Ref: 02-A12771

Diethyl 2-oxomalonate

CAS: 609-09-6

Diethyl 2-oxomalonate

Formula: C₇H₁₀O₅

Purity: 97%

Color and Shape: Yellow Liquid-Clear

Molecular weight: 174.1513

Ref: 54-OR6568

Diethyl 2-oxomalonate

CAS: 609-09-6

Formula: C₇H₁₀O₅

Purity: 97%

Color and Shape: Liquid

Molecular weight: 174.1513

Ref: IN-DA0034QE

Diethyl 2-oxomalonate

CAS: 609-09-6

Diethyl 2-oxomalonate

Formula: C₇H₁₀O₅

Purity: 95%

Molecular weight: 174.15

Ref: IN-DG3829

Diethyl ketomalonate

CAS: 609-09-6

Formula: C₇H₁₀O₅

Purity: 94.0%

Color and Shape: Liquid

Molecular weight: 174.152

Ref: 10-F005421

Diethyl Ketomalonate

Controlled Product

CAS: 609-09-6

Applications Diethyl Ketomalonate (cas# 609-09-6) is a compound useful in organic synthesis.

Formula: C₇H₁₀O₅

Color and Shape: Neat

Molecular weight: 174.15

Ref: TR-D476633

Diethyl ketomalonate

CAS: 609-09-6

Diethyl ketomalonate is an organic compound that is a derivative of malonic acid. It is used as a potent and selective inhibitor of the enzyme protease. Diethyl ketomalonate has been shown to inhibit the activity of a wide range of enzymes, including aminopeptidases, carboxypeptidases, dipeptidases, endopeptidases, esterases, glycosidases, lipase, metalloprotease, peptidase A1, peptidase A2, peptidase M1 and urease. The mechanism of action for this class of compounds involves the formation of an intramolecular hydrogen bond between diethyl ketomalonate and a hydroxyl group in the enzyme's active site. This inhibits catalysis by blocking access to the substrate-binding site.

Formula: C₇H₁₀O₅

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 174.15 g/mol

Ref: 3D-FD10521