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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)-

3(2H)-Furanone, dihydro-2-methyl-

O=C1CCOC1C Request for Quotation
Chemical Name: 3(2H)-Furanone, dihydro-2-methyl-
CAS Number: 3188-00-9
Product Number: AG003UOV(AGN-PC-0JKE51)
Synonyms:
MDL No:
Molecular Formula: C5H8O2
Molecular Weight: 100.1158

Identification/Properties

Properties
BP:
139°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.429(lit.)
Computed Properties
Molecular Weight:
100.117g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
100.052g/mol
Monoisotopic Mass:
100.052g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
88.1
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

GHS Pictogram:
Signal Word:
Danger
UN#:
1224
Hazard Statements:
H226-H302
Precautionary Statements:
P305+P351+P338
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyltetrahydrofuran-3-one, also known as γ-methyl-γ-butyrolactone, is a versatile compound used in various chemical synthesis processes. Its unique structure makes it a valuable building block in organic chemistry, contributing to the creation of a wide range of chemical products. In particular, 2-Methyltetrahydrofuran-3-one is commonly utilized as a solvent in organic reactions due to its ability to dissolve a wide variety of organic and inorganic substances.Moreover, this compound is frequently employed as a precursor in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its presence allows for the formation of complex molecular structures with enhanced properties and functionalities. Additionally, 2-Methyltetrahydrofuran-3-one can serve as a chiral building block, facilitating the synthesis of enantiomerically pure compounds essential in the pharmaceutical industry.Furthermore, its use in the preparation of polymers and materials showcases its significance in modern chemical synthesis. By incorporating 2-Methyltetrahydrofuran-3-one into polymerization reactions, researchers can tailor the properties of the resulting materials, such as solubility, thermal stability, and mechanical strength.Overall, the application of 2-Methyltetrahydrofuran-3-one in chemical synthesis demonstrates its crucial role as a foundational element in the creation of innovative compounds and materials across various industries.