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Home  > 1H-Imidazole-5-methanol, 2-butyl-4-chloro-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, 5-acetate

AA03004

1006062-27-6 | 1H-Imidazole-5-methanol, 2-butyl-4-chloro-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, 5-acetate

Packsize Purity Availability Price Discounted Price    Quantity
20mg 1 week $1,480.00 $1,036.00 -   +

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Description
Catalog Number: AA03004
Chemical Name: 1H-Imidazole-5-methanol, 2-butyl-4-chloro-1-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, 5-acetate
CAS Number: 1006062-27-6
Molecular Formula: C24H25ClN6O2
Molecular Weight: 464.9473
MDL Number: MFCD23160673
SMILES: CCCCc1nc(c(n1Cc1ccc(cc1)c1ccccc1c1n[nH]nn1)COC(=O)C)Cl

 

Upstream Synthesis Route
  • The compound [2-Butyl-4-chloro-1-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate is a versatile molecule that finds widespread use in chemical synthesis. It serves as a valuable building block for creating complex organic compounds due to its unique structure and reactivity.In chemical synthesis, [2-Butyl-4-chloro-1-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate can act as a precursor for the introduction of various functional groups through selective chemical transformations. Its imidazole and tetrazole moieties offer opportunities for further derivatization, enabling the synthesis of diverse organic molecules.Moreover, the presence of the acetate group in [2-Butyl-4-chloro-1-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate allows for facile manipulation under mild reaction conditions. This feature is particularly advantageous in the construction of complex molecular frameworks where precise control over functional group modifications is crucial.Overall, [2-Butyl-4-chloro-1-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate serves as a valuable tool in the hands of synthetic chemists, offering a pathway to access structurally diverse and functionally rich organic compounds through strategic chemical transformations.
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