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Home  > 1H-Benzimidazolium,5,6-dichloro-2-[3-[5,6-dichloro-1-ethyl-1,3-dihydro-3-(4-sulfobutyl)-2H-benzimidazol-2-ylidene]-1-propen-1-yl]-1-ethyl-3-(4-sulfobutyl)-,inner salt

AD48294

10049-96-4 | 1H-Benzimidazolium,5,6-dichloro-2-[3-[5,6-dichloro-1-ethyl-1,3-dihydro-3-(4-sulfobutyl)-2H-benzimidazol-2-ylidene]-1-propen-1-yl]-1-ethyl-3-(4-sulfobutyl)-,inner salt

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Description
Catalog Number: AD48294
Chemical Name: 1H-Benzimidazolium,5,6-dichloro-2-[3-[5,6-dichloro-1-ethyl-1,3-dihydro-3-(4-sulfobutyl)-2H-benzimidazol-2-ylidene]-1-propen-1-yl]-1-ethyl-3-(4-sulfobutyl)-,inner salt
CAS Number: 10049-96-4
Molecular Formula: C29H34Cl4N4O6S2
Molecular Weight: 740.5455
MDL Number: MFCD03093268
SMILES: CCN1C(=CC=Cc2[n+](CCCCS(=O)(=O)[O-])c3c(n2CC)cc(c(c3)Cl)Cl)N(c2c1cc(Cl)c(c2)Cl)CCCCS(=O)(=O)O

 

Upstream Synthesis Route
  • The 1H-Benzimidazolium,5,6-dichloro-2-[3-[5,6-dichloro-1-ethyl-1,3-dihydro-3-(4-sulfobutyl)-2H-benzimidazol-2-ylidene]-1-propen-1-yl]-1-ethyl-3-(4-sulfobutyl)-,inner salt is a versatile compound widely utilized in chemical synthesis. This compound is particularly valuable in the field of organic chemistry for its ability to act as a catalyst in various reactions. Its unique structure allows it to facilitate the formation of complex molecules by promoting key bond formations and structural rearrangements. Researchers and chemists often employ this compound in the construction of new chemical entities and the modification of existing compounds to enhance their properties. Its role in chemical synthesis extends to diverse applications, including the development of pharmaceuticals, agrochemicals, and materials with tailored functionalities.
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