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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)-

2-[[4-(3-methoxypropoxy)-3-methyl-1-oxidopyridin-1-ium-2-yl]methylsulfonyl]-1H-benzimidazole

COCCCOc1cc[n+](c(c1C)CS(=O)(=O)c1nc2c([nH]1)cccc2)[O-] Request for Quotation
Chemical Name: 2-[[4-(3-methoxypropoxy)-3-methyl-1-oxidopyridin-1-ium-2-yl]methylsulfonyl]-1H-benzimidazole
CAS Number: 924663-37-6
Product Number: AG00GTLJ(AGN-PC-00SY6A)
Synonyms:
MDL No:
Molecular Formula: C18H21N3O5S
Molecular Weight: 391.44144

Identification/Properties

Computed Properties
Molecular Weight:
391.442g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
391.12g/mol
Monoisotopic Mass:
391.12g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
570
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


The compound 1H-Benzimidazole, 2-[[[4-(3-methoxypropoxy)-3-methyl-1-oxido-2-pyridinyl]methyl]sulfonyl]- is a versatile chemical reagent commonly used in organic synthesis. It plays a crucial role in the construction of complex molecular structures through various chemical reactions. This compound is particularly valued for its ability to introduce specific functional groups into organic molecules, enabling the synthesis of novel compounds with unique properties. Its sulfonamide group serves as a reactive moiety that can participate in a range of reactions, allowing for the creation of diverse chemical structures with tailored properties. In chemical synthesis, this compound acts as a valuable building block for the preparation of pharmaceuticals, agrochemicals, and materials with advanced functionalities. Its application extends to the development of new catalysts, ligands, and bioactive compounds, making it a valuable tool in the field of synthetic chemistry.