CymitQuimica logo

CAS 22128-99-0

:

1H-Benzimidazole,2-methoxy-

Description:
1H-Benzimidazole, 2-methoxy- is an organic compound characterized by its benzimidazole core, which consists of a fused benzene and imidazole ring. This compound features a methoxy group (-OCH3) attached to the second position of the benzimidazole ring, influencing its chemical properties and reactivity. It is typically a white to off-white solid and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of the methoxy group can enhance its lipophilicity, potentially affecting its biological activity and interactions. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its structure allows for potential hydrogen bonding and π-π stacking interactions, which can be significant in biological systems. As with many benzimidazole derivatives, it may also be involved in coordination chemistry, forming complexes with metal ions. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C8H8N2O
Synonyms:
  • Benzimidazole,2-methoxy- (7CI,8CI)
  • 2-Methoxybenzimidazole
Sort by

Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
  • 2-Methoxy-1H-1,3-benzodiazole

    CAS:
    <p>2-Methoxy-1H-1,3-benzodiazole is a small molecule that has been shown to inhibit the activity of the cyclic AMP response element binding protein. This drug can be used in the treatment of hepatitis C, although it is not effective against other viral infections. 2-Methoxy-1H-1,3-benzodiazole is an antihypertensive agent that has been used in clinical trials for the treatment of diabetic patients and patients with insulin resistance. The mechanism by which this drug exerts its effects on blood pressure is not clear. It may act by decreasing vascular resistance or by increasing cardiac output. 2-Methoxy-1H-1,3-benzodiazole also has anticancer activity and inhibits tumor growth in mice with brain infarction. This compound binds to fatty acids and hydroxyl groups to form a reactive intermediate that reacts with DNA bases to form covalent adduct</p>
    Formula:C8H8N2O
    Purity:Min. 95%
    Molecular weight:148.16 g/mol

    Ref: 3D-XAA12899

    50mg
    344.00€
    500mg
    995.00€