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Home  > Phenol, 2,4-dibromo-6-[[[[(4S,5S)-4,5-dihydro-1-[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1H-imidazol-2-yl]methyl][(1S)-1-phenylethyl]amino]methyl]-

AA04066

1009582-56-2 | Phenol, 2,4-dibromo-6-[[[[(4S,5S)-4,5-dihydro-1-[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1H-imidazol-2-yl]methyl][(1S)-1-phenylethyl]amino]methyl]-

Packsize Purity Availability Price Discounted Price    Quantity
50mg 90.0% 2 weeks $220.00 $154.00 -   +
250mg 90% 2 weeks $776.00 $544.00 -   +
500mg 97% 2 weeks $1,253.00 $877.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA04066
Chemical Name: Phenol, 2,4-dibromo-6-[[[[(4S,5S)-4,5-dihydro-1-[(4-methylphenyl)sulfonyl]-4,5-diphenyl-1H-imidazol-2-yl]methyl][(1S)-1-phenylethyl]amino]methyl]-
CAS Number: 1009582-56-2
Molecular Formula: C38H35Br2N3O3S
Molecular Weight: 773.5758
MDL Number: MFCD22581687
SMILES: Cc1ccc(cc1)S(=O)(=O)N1C(=N[C@H]([C@@H]1c1ccccc1)c1ccccc1)CN([C@H](c1ccccc1)C)Cc1cc(Br)cc(c1O)Br

 

Upstream Synthesis Route
  • The compound 2,4-Dibromo-6-[[[[(4S,5S)-4,5-dihydro-4,5-diphenyl-1-tosyl-1H-imidazol-2-yl]methyl][(S)-1-phenylethyl]amino]methyl]phenol serves as a valuable building block in chemical synthesis due to its unique structure and reactivity. This complex molecule contains multiple functional groups that can participate in various chemical reactions, leading to the formation of diverse products.In chemical synthesis, this compound can be utilized as a key intermediate for the preparation of complex organic molecules. Its substituted imidazole ring provides a versatile platform for the introduction of different functional groups, enabling the synthesis of structurally diverse compounds. The presence of the tosyl group and phenyl groups further enhances the compound's reactivity and compatibility with a wide range of synthetic transformations.Additionally, the amino and hydroxyl groups in 2,4-Dibromo-6-[[[[(4S,5S)-4,5-dihydro-4,5-diphenyl-1-tosyl-1H-imidazol-2-yl]methyl][(S)-1-phenylethyl]amino]methyl]phenol offer opportunities for further derivatization through various coupling reactions, enabling the incorporation of additional functionalities into the synthesized products. Overall, the strategic placement of these functional groups within the molecule makes it a valuable tool for achieving specific structural modifications and enhancing the complexity of organic molecules in chemical synthesis.
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