E35400
Ethyl 2-methylacetoacetate
90%
Synonym(s):
Ethyl 2-methyl-3-oxobutanoate
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3COCH(CH3)CO2C2H5
CAS Number:
Molecular Weight:
144.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-179-9
Beilstein/REAXYS Number:
1071742
MDL number:
Assay:
90%
Form:
liquid
Product Name
Ethyl 2-methylacetoacetate, 90%
InChI key
FNENWZWNOPCZGK-UHFFFAOYSA-N
InChI
1S/C7H12O3/c1-4-10-7(9)5(2)6(3)8/h5H,4H2,1-3H3
SMILES string
CCOC(=O)C(C)C(C)=O
assay
90%
form
liquid
refractive index
n20/D 1.418 (lit.)
bp
187 °C (lit.)
density
1.019 g/mL at 25 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
- Ethyl 2-methylacetoacetate is used as a substrate in the rhenium-catalyzed synthesis of multisubstituted aromatic compounds.
- It can be employed in the synthesis of coumarin derivatives via Pechmann condensation.
- It undergoes dehydration to yield conjugated alkynyl and allenyl esters.
- It is also used in the total synthesis of chlorotonil A, yangjinhualine A, (+)- and (−)-saudin.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
145.4 °F - closed cup
flash_point_c
63 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis of coumarins catalyzed by eco-friendly W/ZrO2 solid acid catalyst.
Reddy B M, et al.
Synthetic Communications, 31(23), 3603-3607 (2001)
Selective One-Pot Synthesis of Allenyl and Alkynyl Esters from β-Ketoesters.
Maity P and Lepore S D
The Journal of Organic Chemistry, 74(1), 158-162 (2008)
Concise, regiocontrolled synthesis of yangjinhualine A.
Boukouvalas J and McCann L C
Tetrahedron Letters, 52(11), 1202-1204 (2011)
K Iwamoto et al.
Bioscience, biotechnology, and biochemistry, 64(1), 194-197 (2000-04-15)
Seven fungi, which are found to reduce ethyl 3-oxobutanoate in high yields, were tested for their reducing ability for ethyl 2-methyl 3-oxobutanoate. We obtained some interesting findings. In particular, Penicillium purpurogenum reduced ethyl 2-methyl 3-oxobutanoate to the corresponding alcohols with
Michal Plž et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-24)
The co-immobilization of ketoreductase (KRED) and glucose dehydrogenase (GDH) on highly cross-linked agarose (sepharose) was studied. Immobilization of these two enzymes was performed via affinity interaction between His-tagged enzymes (six histidine residues on the N-terminus of the protein) and agarose
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service