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  2. 1H-Benzimidazole,5-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-,sodium salt

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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)-

1H-Benzimidazole,5-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-,sodium salt

COc1ccc2c(c1)[nH]c(n2)[S@@](=O)Cc1ncc(c(c1C)OC)C.[Na] Request for Quotation
Chemical Name: 1H-Benzimidazole,5-methoxy-2-[(S)-[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-,sodium salt
CAS Number: 161796-78-7
Product Number: AG001VVZ(AGN-PC-0Q84R8)
Synonyms:
MDL No:
Molecular Formula: C17H19N3NaO3S
Molecular Weight: 368.4058

Identification/Properties

Computed Properties
Molecular Weight:
367.399g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
367.097g/mol
Monoisotopic Mass:
367.097g/mol
Topological Polar Surface Area:
81.5A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
459
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


5-Methoxy-2-((S)-((4-methoxy-3,5-dimethyl-2-pyridyl)methyl)sulfinyl-1H-benzimidazole sodium salt, known for its role in chemical synthesis, exhibits intriguing properties that make it a valuable tool in the laboratory. This compound is commonly utilized as a chiral building block in the asymmetric synthesis of complex organic molecules. By harnessing its stereochemical purity and reactivity, chemists can efficiently introduce chirality into target molecules, enhancing their biological activity and allowing for the creation of novel pharmaceuticals, agrochemicals, and materials. Its strategic incorporation into synthetic pathways enables the creation of diverse molecular architectures with high levels of enantioselectivity, paving the way for the development of cutting-edge compounds with tailored properties and enhanced functionality.