1-tert-butyl 2-methyl indoline-1,2-dicarboxylate

1-tert-butyl 2-methyl indoline-1,2-dicarboxylate

7-nitroindoline hydrochloride

7-nitroindoline hydrochloride

tert-butyl 2-oxoindoline-1-carboxylate

$350.00
CAS No.: 214610-10-3
Catalog No.: 192693
Purity: 95%
MF: C13H15NO3
MW: 233.267
Storage: 2-8 degree Celsius
SMILES: O=C1N(C2=CC=CC=C2C1)C(=O)OC(C)(C)C
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192693
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tert-butyl 2-oxoindoline-1-carboxylate; CAS No.: 214610-10-3; tert-butyl 2-oxoindoline-1-carboxylate. PROPERTIES: This oxo-protected indoline carbamate has molecular formula C12H15N3O3. It typically appears as a white crystalline powder. The tert-butyl 2-oxoindoline-1-carboxylate demonstrates limited water solubility but good solubility in common organic solvents like methanol and ethyl acetate. Its melting point ranges between 130-133 C, and it has a molecular weight of approximately 243.27 g/mol. When handling, care should be taken to avoid skin contact and use of proper respiratory protection. Storage should be in a tightly sealed container at room temperature, protected from light and moisture. The compound is sensitive to strong acids and may undergo carbamate hydrolysis upon exposure to aqueous conditions. In case of spillage, absorb with inert material and dispose of in accordance with local regulations. APPLICATIONS: The tert-butyl 2-oxoindoline-1-carboxylate serves as a key intermediate in the synthesis of dual orexin receptor antagonists for insomnia treatment where the oxo group provides essential hydrogen bonding interactions with receptor subtypes (as reported in medicinal chemistry literature). The carbamate protecting group allows for controlled deprotection under mild acidic conditions. Additionally, the compound functions as a building block in the preparation of chiral ligands for asymmetric catalysis, achieving enantiomeric excesses above 95% in certain hydrogenation reactions as described in synthetic chemistry journals. The carbamate group can be further functionalized through hydrolysis or alkylation reactions to produce various derivatives for chemical research applications.

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