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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)-

Olean-12-ene-3,16,21,22,23,28-hexol, (3b,4a,16b,21b,22a)-

OC[C@]12[C@@H](O)C[C@@]3(C(=CC[C@H]4[C@@]3(C)CC[C@@H]3[C@]4(C)CC[C@@H]([C@@]3(C)CO)O)[C@@H]2CC([C@H]([C@@H]1O)O)(C)C)C Request for Quotation
Chemical Name: Olean-12-ene-3,16,21,22,23,28-hexol, (3b,4a,16b,21b,22a)-
CAS Number: 22467-07-8
Product Number: AG00C4FN(AGN-PC-0QZ1XX)
Synonyms:
MDL No:
Molecular Formula: C30H50O6
Molecular Weight: 506.7144

Identification/Properties

Computed Properties
Molecular Weight:
506.724g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
506.361g/mol
Monoisotopic Mass:
506.361g/mol
Topological Polar Surface Area:
121A^2
Heavy Atom Count:
36
Formal Charge:
0
Complexity:
932
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
12
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Gymnemagenin, a triterpenoid compound derived from the Gymnema sylvestre plant, has found significant application in chemical synthesis due to its unique structural features and biological activities. In the field of organic chemistry, Gymnemagenin serves as a valuable starting material for the synthesis of various bioactive molecules.One key application of Gymnemagenin in chemical synthesis is its role as a precursor for the production of novel pharmaceutical agents. By selectively modifying its chemical structure through reactions such as oxidation, reduction, and functional group manipulation, chemists can create derivatives with enhanced pharmacological properties. These derivatives may exhibit improved bioavailability, increased potency, or modified target specificity, making them promising candidates for drug development.Furthermore, Gymnemagenin's triterpenoid framework offers ample opportunities for structural diversification, allowing chemists to explore diverse synthetic pathways and generate compound libraries for biological screening. This versatile compound can be used as a scaffold for the synthesis of natural product analogs, drug conjugates, or molecular probes, enabling the discovery of new therapeutic agents and research tools.Overall, the application of Gymnemagenin in chemical synthesis showcases its potential as a valuable building block for creating structurally diverse and biologically active compounds. Through strategic transformations and synthetic innovations, this natural product has opened up new avenues for drug discovery and molecular design in the field of medicinal chemistry.