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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)-

Aconitane-7,8-diol,20-ethyl-1,6,14,16-tetramethoxy-4-[[[2-(3-methyl-2,5-dioxo-1-pyrrolidinyl)benzoyl]oxy]methyl]-, [1a,4(S),6b,14a,16b]-,2-hydroxy-1,2,3-propanetricarboxylate (salt)

OC(=O)CC(C(=O)O)(CC(=O)O)O.CCN1C[C@@]2(CC[C@@H]([C@@]34[C@@H]1[C@@](O)([C@H](C23)OC)[C@@]1([C@@H]2[C@H]4C[C@@H]([C@@H]2OC)[C@H](C1)OC)O)OC)COC(=O)c1ccccc1N1C(=O)C[C@@H](C1=O)C Request for Quotation
Chemical Name: Aconitane-7,8-diol,20-ethyl-1,6,14,16-tetramethoxy-4-[[[2-(3-methyl-2,5-dioxo-1-pyrrolidinyl)benzoyl]oxy]methyl]-, [1a,4(S),6b,14a,16b]-,2-hydroxy-1,2,3-propanetricarboxylate (salt)
CAS Number: 112825-05-5
Product Number: AG008Y43(AGN-PC-0P40J0)
Synonyms:
MDL No:
Molecular Formula: C43H58N2O17
Molecular Weight: 874.9238

Identification/Properties

Computed Properties
Molecular Weight:
874.934g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
18
Rotatable Bond Count:
15
Exact Mass:
874.374g/mol
Monoisotopic Mass:
874.374g/mol
Topological Polar Surface Area:
276A^2
Heavy Atom Count:
62
Formal Charge:
0
Complexity:
1610
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
13
Undefined Atom Stereocenter Count:
1
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


Methyllycaconitine citrate, a potent alkaloid compound derived from Aconitum plants, serves as a valuable tool in chemical synthesis due to its unique properties. This specialized chemical reagent finds application as a chiral building block in asymmetric synthesis, particularly in the formation of complex organic molecules with high enantioselectivity. By leveraging the specific structure and reactivity of Methyllycaconitine citrate, chemists can achieve precise control over the stereochemistry of their synthetic pathways, enabling the creation of intricate molecular architectures with enhanced biological activity or pharmaceutical potential. Furthermore, the strategic incorporation of Methyllycaconitine citrate into synthetic routes can facilitate the development of novel drug candidates, agrochemicals, and materials with improved performance characteristics. In essence, Methyllycaconitine citrate plays a pivotal role in advancing the frontiers of chemical synthesis by enabling the efficient and selective construction of molecular frameworks with diverse applications in various scientific disciplines.