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CAS 380629-73-2

:

1,1-Dimethylethyl N-(5-amino-1,2-benzisoxazol-3-yl)carbamate

Description:
1,1-Dimethylethyl N-(5-amino-1,2-benzisoxazol-3-yl)carbamate, identified by its CAS number 380629-73-2, is a chemical compound characterized by its unique structure that includes a carbamate functional group and a benzisoxazole moiety. This compound typically exhibits properties associated with both the carbamate and benzisoxazole functionalities, such as potential biological activity and solubility in organic solvents. The presence of the dimethyl group contributes to its steric hindrance, which may influence its reactivity and interaction with biological targets. The amino group on the benzisoxazole ring can participate in hydrogen bonding, enhancing its potential as a pharmacophore in medicinal chemistry. Overall, this compound may be of interest in research fields such as drug development, particularly for its potential therapeutic applications, although specific biological activities and mechanisms would require further investigation. Safety and handling precautions should be observed, as with any chemical substance, due to the potential for toxicity or reactivity.
Formula:C12H15N3O3
InChI:InChI=1S/C12H15N3O3/c1-12(2,3)17-11(16)14-10-8-6-7(13)4-5-9(8)18-15-10/h4-6H,13H2,1-3H3,(H,14,15,16)
InChI key:InChIKey=VKHZQNDFOLJRBM-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C=1C=2C(ON1)=CC=C(N)C2
Synonyms:
  • Carbamic acid, (5-amino-1,2-benzisoxazol-3-yl)-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl N-(5-amino-1,2-benzisoxazol-3-yl)carbamate
  • tert-Butyl N-(5-aminobenzisoxazol-3-yl)carbamate
  • Carbamic acid, N-(5-amino-1,2-benzisoxazol-3-yl)-, 1,1-dimethylethyl ester
  • (5-Aminobenzo[d]isoxazol-3-yl)carbamic acid tert-butyl ester
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