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CAS 29711-79-3

:

4-Isothiocyanato-N,N-dimethyl-1-naphthalenamine

Description:
4-Isothiocyanato-N,N-dimethyl-1-naphthalenamine, with the CAS number 29711-79-3, is an organic compound characterized by the presence of both isothiocyanate and naphthalene functional groups. This compound typically appears as a solid and is known for its reactivity due to the isothiocyanate group, which can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. The presence of the dimethylamino group enhances its solubility in organic solvents and may influence its biological activity. This compound is of interest in the field of organic synthesis and may have applications in the development of agrochemicals or pharmaceuticals. Additionally, its structural features suggest potential interactions with biological systems, making it a candidate for further research in medicinal chemistry. Safety data should be consulted, as isothiocyanates can be irritants and may pose health risks if not handled properly. Overall, 4-Isothiocyanato-N,N-dimethyl-1-naphthalenamine is a versatile compound with significant implications in various chemical and biological contexts.
Formula:C13H12N2S
InChI:InChI=1S/C13H12N2S/c1-15(2)13-8-7-12(14-9-16)10-5-3-4-6-11(10)13/h3-8H,1-2H3
InChI key:InChIKey=SMZHGTXTWIAKGS-UHFFFAOYSA-N
SMILES:N(C)(C)C=1C2=C(C(N=C=S)=CC1)C=CC=C2
Synonyms:
  • 1-Naphthalenamine, 4-isothiocyanato-N,N-dimethyl-
  • 4-(Dimethylamino)-1-naphthyl isothiocyanate
  • 4-Isothiocyanato-N,N-dimethyl-1-naphthalenamine
  • 4-N,N-Dimethylamino-1-naphthylisothiocyanate
  • Isothiocyanic acid, 4-(dimethylamino)-1-naphthyl ester
  • 4-Isothiocyanato-N,N-dimethylnaphthalen-1-amine
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