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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-Furancarboxylic acid, 4,5-dihydro-

OC(=O)C1=COCC1 Request for Quotation
Chemical Name: 3-Furancarboxylic acid, 4,5-dihydro-
CAS Number: 98021-62-6
Product Number: AG00IK0L(AGN-PC-0JT5BV)
Synonyms:
MDL No:
Molecular Formula: C5H6O3
Molecular Weight: 114.0993

Identification/Properties

Computed Properties
Molecular Weight:
114.1g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
114.032g/mol
Monoisotopic Mass:
114.032g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
137
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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:
Warning
UN#:
-
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dihydrofuran-3-carboxylic acid is a versatile compound commonly utilized in chemical synthesis as a key building block for creating various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it a valuable intermediate in the production of a wide range of organic compounds.In chemical synthesis, 4,5-Dihydrofuran-3-carboxylic acid can undergo a variety of transformations to introduce functional groups or modify its structure. It can be used as a starting material in the synthesis of heterocyclic compounds, which are crucial in the pharmaceutical industry for their diverse biological activities. By reacting with different reagents or catalysts, this compound can be transformed into derivatives with enhanced properties or specific functionalities.Furthermore, the presence of the carboxylic acid group in 4,5-Dihydrofuran-3-carboxylic acid allows for easy modification through various chemical reactions such as esterification, amidation, or condensation reactions. This flexibility enables chemists to tailor the compound to meet the specific requirements of a target molecule, making it an important tool in the design and synthesis of complex organic molecules.Overall, 4,5-Dihydrofuran-3-carboxylic acid plays a crucial role in chemical synthesis by serving as a versatile and customizable building block for the construction of diverse organic compounds with potential applications in various industries.