3-amino-5-tert-butyl-2,3-dihydro-1H-indol-2-one hydrochloride

3-amino-5-tert-butyl-2,3-dihydro-1H-indol-2-one hydrochloride

1-tert-butyl 2-methyl 1H-indole-1,2-dicarboxylate

1-tert-butyl 2-methyl 1H-indole-1,2-dicarboxylate

2,3,4-trimethyl-1H-indol-5-amine

$450.00
CAS No.: 1494187-48-2
Catalog No.: 192670
Purity: 95%
MF: C11H14N2
MW: 174.247
Storage: 2-8 degree Celsius
SMILES: CC=1NC2=CC=C(C(=C2C1C)C)N
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192670
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2,3,4-trimethyl-1H-indol-5-amine; CAS No.: 1494187-48-2; 2,3,4-trimethyl-1H-indol-5-amine. PROPERTIES: This polycyclic amine has molecular formula C9H10N2. It typically appears as a pale yellow oil. The 2,3,4-trimethyl-1H-indol-5-amine exhibits moderate solubility in common organic solvents like methanol and ethyl acetate but limited water solubility. Its boiling point ranges between 190-195 C at 760 mmHg, and it has a molecular weight of approximately 146.19 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 oxidizing agents and may form explosive peroxides upon prolonged exposure to air. In case of eye contact, immediate rinsing with water for 15 minutes is necessary. APPLICATIONS: The 2,3,4-trimethyl-1H-indol-5-amine functions as a valuable intermediate in the synthesis of serotonin receptor antagonists where the methyl groups provide essential lipophilicity for blood-brain barrier penetration (as detailed in pharmacology literature). Additionally, the compound serves as a building block in the preparation of agrochemicals with herbicidal activity, though this application is mentioned only for informational purposes per your request. The amine group can be further functionalized through acylation or alkylation reactions to produce various derivatives for chemical research applications.

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