Biosynth

1,2-Dihydro-3H-indol-3-one, also known as indolin-2-one, is an organic compound characterized by its bicyclic structure, which consists of an indole ring fused with a carbonyl group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO). It exhibits a range of interesting chemical properties, including the ability to participate in various chemical reactions such as electrophilic substitutions and cycloadditions. The presence of the carbonyl group contributes to its reactivity, making it a valuable intermediate in organic synthesis. Additionally, 1,2-dihydro-3H-indol-3-one has garnered attention in medicinal chemistry due to its potential biological activities, including anti-inflammatory and anticancer properties. Its derivatives are often explored for their pharmacological applications, highlighting the compound's significance in both synthetic and medicinal chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, following appropriate safety protocols.

1,2-Dihydro-3H-indol-3-one

3260-61-5: 1,2-Dihydro-3H-indol-3-one, also known as indolin-2-one, is an organic compound characterized by its bicyclic structure, which consists of an indole ring fused with a carbonyl group. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO). It exhibits a range of interesting chemical properties, including the ability to participate in various chemical reactions such as electrophilic substitutions and cycloadditions. The presence of the carbonyl group contributes to its reactivity, making it a valuable intermediate in organic synthesis. Additionally, 1,2-dihydro-3H-indol-3-one has garnered attention in medicinal chemistry due to its potential biological activities, including anti-inflammatory and anticancer properties. Its derivatives are often explored for their pharmacological applications, highlighting the compound's significance in both synthetic and medicinal chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, following appropriate safety protocols.

3-Hydroxyindole is a chemical compound that is used in the synthesis of coumarin derivatives. It can be synthesized from 3-methoxyindole by treatment with trifluoroacetic acid and potassium dichromate, followed by hydrolysis of the resulting 3-hydroxyindole with sodium carbonate. It has been shown to have anti-inflammatory properties and may be useful for the treatment of chronic cough and asthma. The pharmacokinetics of 3-hydroxyindole have been extensively studied in humans and animals. The half-life of 3-hydroxyindole is approximately 2 hours and it is eliminated primarily through renal excretion. This drug also binds to opioid receptors and has been shown to have intramolecular hydrogen bonds.

CAS 3260-61-5

1,2-Dihydro-3H-indol-3-one

Indolin-3-one

Ref: 3D-DAA26061