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AI53706

615-16-7 | 2-Hydroxybenzimidazole

Packsize Purity Availability Price Discounted Price    Quantity
10g 99% in stock $8.00 $5.00 -   +
25g 99% in stock $15.00 $10.00 -   +
100g 99% in stock $29.00 $20.00 -   +

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*All prices are in USD.

Description
Catalog Number: AI53706
Chemical Name: 2-Hydroxybenzimidazole
CAS Number: 615-16-7
Molecular Formula: C7H6N2O
Molecular Weight: 134.13534
MDL Number: MFCD00127894
SMILES: O=c1[nH]c2c([nH]1)cccc2

 

Computed Properties
Complexity: 142  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 2  
XLogP3: 1.1  

 

 

Upstream Synthesis Route
  • 2-Hydroxybenzimidazole, also known as salicylimidazole, is a versatile compound widely utilized in chemical synthesis. Its unique structure and properties make it a valuable component in various reactions and processes within the field of chemistry.In chemical synthesis, 2-Hydroxybenzimidazole serves as a crucial building block for the creation of many organic compounds. It can participate in condensation reactions to form heterocyclic ring structures, lending its aromatic character to the final product. The hydroxyl group presents in 2-Hydroxybenzimidazole enables it to engage in hydrogen bonding interactions, leading to the formation of complex molecular architectures with enhanced properties.Furthermore, 2-Hydroxybenzimidazole is often employed as a precursor in the synthesis of pharmaceutical compounds, agrochemicals, and specialty chemicals. Its presence in the synthesis pathway can dictate the stereochemistry and functional group arrangements in the final product, influencing its biological or chemical activity. By incorporating 2-Hydroxybenzimidazole into the synthesis route, chemists can achieve targeted modifications and optimize the desired properties of the end product.Overall, the application of 2-Hydroxybenzimidazole in chemical synthesis extends beyond a mere reagent; it acts as a strategic intermediate that imparts specific characteristics and functionalities to diverse molecules, thereby expanding the scope of synthesis possibilities for chemists across various disciplines.
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