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Home  > (4-Bromo-1-methyl-1h-benzoimidazol-2-yl)-methanol

AA20316

1150618-44-2 | (4-Bromo-1-methyl-1h-benzoimidazol-2-yl)-methanol

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% in stock $196.00 $137.00 -   +
100mg 95% in stock $322.00 $225.00 -   +
250mg 95% in stock $546.00 $382.00 -   +
1g 95% in stock $1,334.00 $934.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA20316
Chemical Name: (4-Bromo-1-methyl-1h-benzoimidazol-2-yl)-methanol
CAS Number: 1150618-44-2
Molecular Formula: C9H9BrN2O
Molecular Weight: 241.0846
MDL Number: MFCD12031288
SMILES: OCc1nc2c(n1C)cccc2Br

 

Computed Properties
Complexity: 191  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • The compound 4-Bromo-1-methyl-1H-benzimidazole-2-methanol is a versatile building block in chemical synthesis due to its unique structure and reactivity. As a substituted benzimidazole derivative, it offers a wide range of applications in the preparation of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 4-Bromo-1-methyl-1H-benzimidazole-2-methanol can serve as a key intermediate for the synthesis of various biologically active compounds. The bromine and methyl substituents on the benzimidazole ring can participate in a variety of synthetic transformations, allowing for the introduction of additional functional groups or modifications to tailor the structure for specific desired properties.Additionally, the presence of the hydroxyl group on the benzimidazole ring provides a site for further derivatization or functionalization, enabling the attachment of other molecular fragments to enhance the compound's biological activity or chemical reactivity. Its unique structure makes it a valuable tool for medicinal chemists and synthetic organic chemists seeking to develop novel compounds with potential applications in drug discovery or material science research.
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