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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-Furanamine, tetrahydro-, (R)-, 4-methylbenzenesulfonate

Cc1ccccc1S(=O)(=O)O.N[C@H]1COCC1 Request for Quotation
Chemical Name: 3-Furanamine, tetrahydro-, (R)-, 4-methylbenzenesulfonate
CAS Number: 111769-27-8
Product Number: AG0081SV(AGN-PC-0NXQWC)
Synonyms:
MDL No:
Molecular Formula: C11H17NO4S
Molecular Weight: 259.3220

Identification/Properties

Computed Properties
Molecular Weight:
259.32g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
259.088g/mol
Monoisotopic Mass:
259.088g/mol
Topological Polar Surface Area:
98A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
253
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-Tetrahydrofuran-3-amine 4-methylbenzenesulfonate, a versatile compound widely utilized in chemical synthesis, plays a pivotal role in the development of various pharmaceuticals, agrochemicals, and advanced materials. By serving as a key intermediate in the synthesis of bioactive molecules, this compound enables the creation of complex structures and functional groups essential for a wide range of applications. Its unique reactivity and stereochemistry make it particularly valuable in asymmetric synthesis and the production of chiral compounds. Additionally, (R)-Tetrahydrofuran-3-amine 4-methylbenzenesulfonate exhibits excellent stability and selectivity, making it a favored building block for designing novel chemical entities with enhanced properties and biological activities.