Methyl 6-chlorooxoindoline-3-carboxylate, with the CAS number 151056-78-9, is a chemical compound that belongs to the class of oxoindoles, which are characterized by their indole structure featuring a carbonyl group. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. The presence of the chloro substituent can influence its reactivity and solubility, making it a subject of interest in synthetic organic chemistry. Methyl esters, like this compound, often display moderate to high lipophilicity, which can affect their bioavailability and pharmacokinetic properties. Additionally, the compound may undergo various chemical reactions, such as hydrolysis or substitution, depending on the conditions, which can be leveraged in synthetic pathways for further functionalization. As with many chemical substances, safety data and handling precautions should be observed due to potential toxicity or reactivity.

METHYL 6-CHLOROOXOINDOLINE-3-CARBOXYLATE

151056-78-9: Methyl 6-chlorooxoindoline-3-carboxylate, with the CAS number 151056-78-9, is a chemical compound that belongs to the class of oxoindoles, which are characterized by their indole structure featuring a carbonyl group. This compound typically exhibits a pale yellow to off-white crystalline appearance. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. The presence of the chloro substituent can influence its reactivity and solubility, making it a subject of interest in synthetic organic chemistry. Methyl esters, like this compound, often display moderate to high lipophilicity, which can affect their bioavailability and pharmacokinetic properties. Additionally, the compound may undergo various chemical reactions, such as hydrolysis or substitution, depending on the conditions, which can be leveraged in synthetic pathways for further functionalization. As with many chemical substances, safety data and handling precautions should be observed due to potential toxicity or reactivity.

CAS 151056-78-9

METHYL 6-CHLOROOXOINDOLINE-3-CARBOXYLATE

6-Chloro-2-oxo-2,3-dihydro-1h-indole-3-carboxylic acid methyl ester

Ref: IN-DA001N1R

METHYL 6-CHLOROOXOINDOLINE-3-CARBOXYLATE

Ref: 10-F303337