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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, tetrahydro-, methyl ester, (R)-

COC(=O)[C@H]1COCC1 Request for Quotation
Chemical Name: 3-Furancarboxylic acid, tetrahydro-, methyl ester, (R)-
CAS Number: 191347-93-0
Product Number: AG002F63(AGN-PC-0O65PM)
Synonyms:
MDL No:
Molecular Formula: C6H10O3
Molecular Weight: 130.1418

Identification/Properties

Computed Properties
Molecular Weight:
130.143g/mol
XLogP3:
0.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
130.063g/mol
Monoisotopic Mass:
130.063g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
111
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-Methyl tetrahydrofuran-3-carboxylate is a versatile compound widely used in chemical synthesis for its unique structural and reactivity properties. In organic chemistry, this compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its cyclic structure and ester functionality make it a valuable intermediate in the formation of complex molecular structures.One of the main applications of (R)-Methyl tetrahydrofuran-3-carboxylate is in asymmetric synthesis, where it can be utilized as a chiral auxiliary or a chiral starting material to introduce chirality into target molecules. By leveraging the stereochemistry of this compound, chemists can create enantiomerically pure products, which is crucial in drug development and other areas requiring highly specific molecular structures.Additionally, (R)-Methyl tetrahydrofuran-3-carboxylate can participate in various chemical transformations such as ring-opening reactions, esterifications, and coupling reactions. Its versatility allows for the introduction of functional groups at specific positions in a molecule, enabling the synthesis of diverse chemical compounds with tailored properties.Overall, the application of (R)-Methyl tetrahydrofuran-3-carboxylate in chemical synthesis offers a powerful tool for designing and constructing complex molecules with precision and control, making it an invaluable resource in the field of organic chemistry.