Ethyl 3-methyl-2-oxobutyrate - CAS 20201-24-5

Name: Ethyl 3-methyl-2-oxobutyrate
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB015711
Product Name:	Ethyl 3-methyl-2-oxobutyrate
CAS:	20201-24-5
Synonyms:	ethyl 3-methyl-2-oxobutanoate

Technical Data

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Computed Properties

IUPAC Name:	ethyl 3-methyl-2-oxobutanoate
Description:	Ethyl 3-methyl-2-oxobutyrate (CAS# 20201-24-5 ) is a useful research chemical.
Molecular Weight:	144.17
Molecular Formula:	C7H12O3
Canonical SMILES:	CCOC(=O)C(=O)C(C)C
InChI:	InChI=1S/C7H12O3/c1-4-10-7(9)6(8)5(2)3/h5H,4H2,1-3H3
InChI Key:	CKTYYUQUWFEUCO-UHFFFAOYSA-N
Boiling Point:	62 °C
Purity:	95 %
Density:	0.989 g/cm³
Appearance:	Clear light yellow liquid
MDL:	MFCD00009122
LogP:	0.77460

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Related Functional Groups

Carbonyl Compounds

[91125-43-8]C15H22O5S.Na
Sulfophenyl nonanoate sodium salt
[89908-23-6]C23H22N2O5
2-Propenoic acid, 2-(3',3'-dimethyl-6-nitrospiro[2H-1-benzopyran-2,2'-[2H]indol]-1'(3'H)-yl)ethyl ester
[5650-34-0]C9H8O2
Oxiran-2-yl(phenyl)methanone
[51493-02-8]C5H10ClNO
N-Methyl-N-propylcarbamoyl Chloride
[70199-62-1]C8H10ClNO
(4-Pyridyl)acetone Hydrochloride
[956439-56-8]C6H5N3O6
1-(Carboxymethyl)-3-nitro-1H-pyrazole-5-carboxylic acid

GHS Hazard Statement:	H226 (100%): Flammable liquid and vapor [Warning Flammable liquids]
Precautionary Statement:	P210, P233, P240, P241, P242, P243, P280, P303+P361+P353, P370+P378, P403+P235, and P501
Signal Word:	Warning

Publication Number	Title	Priority Date
WO-2021187411-A1	Animal cell culturing method	20200316
US-2020331941-A1	Organic electroluminescent materials and devices	20190422
PL-236364-B1	8-Substituted-3- (propan-2-yl) -7,8-dihydroimidazo [2,1-c] [1,2,4] triazin-4 (6H) -ones, their preparation and medical use	20190306
FR-3083140-A1	Catalyst based on a c5 or c6 acid ester and its use in a hydroprocessing and / or hydrocracking process	20180627
WO-2020002138-A1	C5 or c6 acid ester-based catalyst and use thereof in a hydroprocessing and/or hydrocracking process	20180627

PMID	Publication Date	Title	Journal
17151458	20061201	Stereoselective reduction of carbonyl compounds using the cell-free extract of the earthworm, Lumbricus rubellus, as a novel source of biocatalyst	Bioscience, biotechnology, and biochemistry
12005054	20020301	Purification and characterization of two alpha-keto ester reductases from Streptomyces thermocyaneoviolaceus IFO 14271	Bioscience, biotechnology, and biochemistry

Complexity:	138
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	144.078644241
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	144.078644241
Rotatable Bond Count:	4
Topological Polar Surface Area:	43.4 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.4