CAS 133-13-1

1,3-Diethyl 2-ethylpropanedioate

Description:

1,3-Diethyl 2-ethylpropanedioate, with the CAS number 133-13-1, is an organic compound belonging to the class of diesters. It features a central propanedioate structure with ethyl groups attached to both the 1 and 3 positions, as well as an additional ethyl group at the 2 position. This compound is typically a colorless to pale yellow liquid with a fruity odor, indicative of its ester nature. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic alkyl chains. The compound is often used in organic synthesis and as an intermediate in the production of various chemicals. Its reactivity is characterized by the presence of ester functional groups, making it susceptible to hydrolysis and transesterification reactions. Safety data indicates that, like many esters, it should be handled with care, as it may cause irritation upon contact with skin or eyes. Proper storage in a cool, dry place away from strong oxidizing agents is recommended to maintain its stability.

Formula: C₉H₁₆O₄

InChI: InChI=1/C9H16O4/c1-4-7(8(10)12-5-2)9(11)13-6-3/h7H,4-6H2,1-3H3

InChI key: InChIKey=VQAZCUCWHIIFGE-UHFFFAOYSA-N

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

Synonyms:

• 1,3-Diethyl 2-ethylpropanedioate
• 2-Ethylmalonic acid diethyl ester
• Diethyl 2-ethylmalonate
• Diethyl Ethylpropanedioate
• Diethyl α-ethylmalonate
• Ethylmalonic acid diethyl ester
• Ethylpropanedioic acid diethyl ester
• Malonic acid, ethyl-, diethyl ester
• NSC 8706
• Propanedioic acid, 2-ethyl-, 1,3-diethyl ester
• Propanedioic acid, ethyl-, diethyl ester
• Diethyl ethylmalonate
• ethyl-propanedioicacidiethylester
• Diethylethylmalonat
• ethyl-propanedioicaciddiethylester
• Ethylmalonicacid,diethylest
• 2-ethyl-malonicaciddiethylester
• Ethylmalonicester
• Diethyl 2-ethylpropanedioate
• 2-Ethylpropanedioic acid diethyl ester
• DIETHYL ETHYLAMAONATE
• DEEM

Propanedioic acid, 2-ethyl-, 1,3-diethyl ester

CAS: 133-13-1

Formula: C₉H₁₆O₄

Purity: 98%

Color and Shape: Liquid

Molecular weight: 188.2209

Ref: IN-DA0011HG

Diethyl Ethylmalonate

CAS: 133-13-1

Diethyl Ethylmalonate

Purity: 98%

Molecular weight: 188.22g/mol

Ref: 54-OR1030690

Diethyl ethylmalonate

CAS: 133-13-1

Formula: C₉H₁₆O₄

Purity: (GC) ≥ 99.0%

Color and Shape: Clear, colourless liquid

Molecular weight: 188.22

Ref: 7W-GK0564

1,3-Diethyl 2-ethylpropanedioate

CAS: 133-13-1

1,3-Diethyl 2-ethylpropanedioate

Purity: 95%

Molecular weight: 188.22g/mol

Ref: 54-OR79849

Diethyl Ethylmalonate

CAS: 133-13-1

Formula: C₉H₁₆O₄

Purity: >98.0%(GC)

Color and Shape: Colorless to Almost colorless clear liquid

Molecular weight: 188.22

Ref: 3B-E0138

Diethyl Ethylmalonate

Controlled Product

CAS: 133-13-1

Applications Diethyl Ethylmalonate is used in the synthesis of HIV-1 reverse transcriptase inhibitors. Also used in the preparation of Peloruside A, a novel antimitotic agent used as a potential anti-cancer agent.
References Wu, H. et al.: Bioorg. Med. Chem., 21, 6477 (2013); Hood, L. et al.: Cancer Res., 62, 3356 (2002);

Formula: C₉H₁₆O₄

Color and Shape: Neat

Molecular weight: 188.22

Ref: TR-D444305

Diethyl 2-ethylmalonate

CAS: 133-13-1

Formula: C₉H₁₆O₄

Purity: 97%

Color and Shape: Liquid

Molecular weight: 188.223

Ref: 10-F464286

Diethyl Ethylmalonate

CAS: 133-13-1

Diethyl ethylmalonate is a chemical compound that belongs to the group of polycarboxylic acids. It is primarily used as a solvent for coatings and adhesives, as well as a catalyst in the Friedel-Crafts reaction. Diethyl ethylmalonate has been shown to undergo a number of reactions, often in the presence of chlorine or another halogen atom. This compound reacts with malonic acid to form diethyl succinate, which can be hydrolyzed by water to form carbon dioxide and ethanol. Diethyl ethylmalonate also binds to receptors on cells, which may be related to its viscosity. The reactivity of this compound can be controlled by varying the particle size.

Formula: C₉H₁₆O₄

Purity: Min. 95%

Molecular weight: 188.22 g/mol

Ref: 3D-AAA13313