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Ethyl 2-methylacetoacetate, 95%, Thermo Scientific Chemicals
Catalog number: A11629.36
500 g, Each
Thermo Scientific Chemicals
Ethyl 2-methylacetoacetate, 95%, Thermo Scientific Chemicals
Catalog number: A11629.36
500 g, Each
Quantity
Catalog number: A11629.36
also known as A11629-36
Price (USD)
Price: 450.00
Online price: 385.65
Your price:
Quantity
-
Chemical Identifiers
CAS
609-14-3
IUPAC Name
ethyl 2-methyl-3-oxobutanoate
Molecular Formula
C7H12O3
InChI Key
FNENWZWNOPCZGK-UHFFFAOYNA-N
SMILES
CCOC(=O)C(C)C(C)=O
Specifications
Specification SheetAssay (GC)
≥94.0%
Form
Liquid
Refractive Index
1.4155-1.4215 @ 20?C
Appearance (Color)
Clear colorless to yellow
Description
Ethyl 2-methylacetoacetate is used in Japp-Klingemann reaction to prepare hydrazones from beta-keto acid and aryl diazonium salts. It is used as a precursor involved in the synthesis of ethylpyruvate phenylhydrazone via reaction with benzenediazonium chloride.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Ethyl 2-methylacetoacetate is used in Japp-Klingemann reaction to prepare hydrazones from beta-keto acid and aryl diazonium salts. It is used as a precursor involved in the synthesis of ethylpyruvate phenylhydrazone via reaction with benzenediazonium chloride.
Solubility
Miscible with alcohol and ether. Silghtly miscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
Ethyl 2-methylacetoacetate is used in Japp-Klingemann reaction to prepare hydrazones from beta-keto acid and aryl diazonium salts. It is used as a precursor involved in the synthesis of ethylpyruvate phenylhydrazone via reaction with benzenediazonium chloride.
Solubility
Miscible with alcohol and ether. Silghtly miscible with water.
Notes
Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
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