2-Amino-5-methoxyphenol, with the CAS number 40925-70-0, is an organic compound characterized by the presence of an amino group (-NH2) and a methoxy group (-OCH3) attached to a phenolic ring. This compound typically appears as a solid and is soluble in polar solvents due to its functional groups. The amino group contributes to its basicity, while the methoxy group can influence its reactivity and solubility. 2-Amino-5-methoxyphenol is often used in various applications, including as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. Its phenolic structure may also impart antioxidant properties. The compound's stability can be affected by environmental factors such as pH and temperature, and it may undergo oxidation or other chemical transformations under certain conditions. Safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled. Overall, 2-Amino-5-methoxyphenol is a versatile compound with significant relevance in organic chemistry and industrial applications.

2-Amino-5-methoxyphenol

40925-70-0: 2-Amino-5-Methoxyphenol, 2-Hydroxy-4-methoxyaniline, 5-Methoxy-2-aminophenol, Phenol, 2-amino-5-methoxy-

2-Amino-5-methoxyphenol is a monomer that has biological properties. It is a nucleophile and can react with copper to form a complex. 2-Amino-5-methoxyphenol also can bind to the antibody of the monoclonal type. This property makes it an ideal candidate for use in cancer treatments. 2-Amino-5-methoxyphenol has been shown to inhibit cellular transformation in both animal and human tissue cells, as well as induce apoptosis in prostate cancer cells. It also inhibits the growth of breast cancer cells by inducing G1 arrest, which prevents replication of DNA and cell division.

CAS 40925-70-0: 2-Amino-5-methoxyphenol

2-Amino-5-methoxyphenol

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2-Amino-5-methoxyphenol

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