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Detail of "6232-92-4"

  • CAS Number:
  • 6232-92-4
  • Name:
  • 1H-Benzimidazol-2-amine,6-nitro-

  • Superlist Name:
  • 2-Amine-5-nitro-1H-benzimidazole
  • Molecular Structure:
  • Formula:
  • C7H6N4O2
  • Molecular Weight:
  • 178.15
  • Synonyms:
  • 1H-Benzimidazol-2-amine,5-nitro- (9CI);2-Amino-5-nitrobenzimidazole;2-Amino-6-nitrobenzimidazole;5-Nitro-2-benzimidazolamine;NSC 287065;
  • Density:
  • 1.631 g/cm3
  • Boiling Point:
  • 478.5 °C at 760 mmHg
  • Flash Point:
  • 243.2 °C

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CAS No.6232-92-4 2-Amine-5-nitro-1H-benzimidazole

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CAS No.6232-92-4 2-Amine-5-nitro-1H-benzimidazole

2-AMINO-5-NITRO-1H-BENZIMIDAZOLE

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CAS No.6232-92-4 2-Amine-5-nitro-1H-benzimidazole

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Reference

Synthesis, crystal structure determination, and antiproliferative evaluation of novel benzazolyl benzamides
All Rights Reserved. Synthesis, crystal structure determination, and antiproliferative evaluation of novel benzazolyl benzamides. Starcevic, Kristina; Caleta, Irena; Cincic, Dominik; Kaitner, Branko; Kralj, Marijeta; Ester, Katja; Karminski-Zamola, Grace (Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, Zagreb HR-10000, Croatia). Heterocycles, 68(11), 2285-2299 (English) 2006 Japan Institute of Heterocyclic Chemistry. CODEN: HTCYAM. ISSN: 0385-5414. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1, 75 A series of N-benzazolylbenzamides contg. different substituents were synthesized by condensation of 2-aminobenzazoles with 4-substituted benzoyl chlorides. All compds. were characterized by IR, 1H and 13C NMR, MS, and elemental anal. The crystal structure of 4-cyano-N-benzothiazol-2-ylbenzamide is presented [monoclinic, space group C2/c, a 30.257(3), b 7.9545(8), c 11.3393(14) ?, b 103.26(1)°, V 2656.35(65) ?3, Z 8]. Some of the new synthesized compds. 6232-92-4 and 934-32-7 are just another two chemicals used in this study. were screened for antitumor activities and showed accentuated in-vitro growth inhibitory activity on human cancer cell lines. .
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