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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

ethyl 3-oxo-3-(oxolan-2-yl)propanoate

CCOC(=O)CC(=O)C1CCCO1 Request for Quotation
Chemical Name: ethyl 3-oxo-3-(oxolan-2-yl)propanoate
CAS Number: 887411-85-0
Product Number: AG003Q8E(AGN-PC-03VBN8)
Synonyms:
MDL No: MFCD06410652
Molecular Formula: C9H14O4
Molecular Weight: 186.2051

Identification/Properties

Properties
BP:
268.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
186.207g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
186.089g/mol
Monoisotopic Mass:
186.089g/mol
Topological Polar Surface Area:
52.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
200
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 3-oxo-3-(tetrahydrofuran-2-yl)propanoate, commonly known as $name$, serves as a versatile building block in chemical synthesis. This compound is utilized as a key intermediate in the preparation of various organic compounds and pharmaceuticals. Its unique structure allows for the introduction of functional groups and modifications that are essential in the synthesis of complex molecules. In addition, $name$ exhibits reactivity that enables it to participate in a range of organic reactions, making it a valuable tool for organic chemists seeking to design and create new compounds with specific properties.