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Home > Encyclopedia > 1,3-bits(2-benzimidazolyl)benzene

1,3-bits(2-benzimidazolyl)benzene

1,3-bits(2-benzimidazolyl)benzene structure

1,3-bits(2-benzimidazolyl)benzene 

structure
  • CAS No:

    29914-81-6

  • Formula:

    C20H14N4

  • Chemical Name:

    1,3-bits(2-benzimidazolyl)benzene

  • Synonyms:

    1,3-bits(2-benzimidazolyl)benzene;1,3-Bis(2-benzimidazolyl)benzene;1,3-Di(1H-benzo[d]imidazol-2-yl)benzene;1,3-Bis(1H-benzo[d]iMidazol-2-yl)benzene;2,2'-(1,3-phenylene)bis-1H-Benzimidazole;1,3-Bis(1H-benzo[d]imidazol-2-yl)

  • Categories:

    Pharmaceutical Intermediates  >  Heterocyclic Compound

1,3-bits(2-benzimidazolyl)benzene Basic Attributes

310.359

310.121857

133357

DTXSID10299862

2933990090

Characteristics

57.4

4.5

1.3±0.1 g/cm3

633.3°C at 760 mmHg

295.1±27.2 °C

1.770

6.05E-16mmHg at 25°C

Safety Information

IRRITANT

1,3-bits(2-benzimidazolyl)benzene Use and Manufacturing

Isophthalic acid (1.130 g, 6.8 mmol) and 1, 2-diaminobenzene (1.417 g, 13.1 mmol) were dissolved in 20 mL of polyphosphoric acid. The stirred mixture was maintained at 190 °C for 24 h. The solution was allowed to cool at room temperature (20 – 25 °C) and slowly stirred in 50 mL of ice. The reaction mixture was neutralized with NaOH and the precipitate was filtered out and washed with cold water. The solid was recrystallized from methanol to yield a white-off solid (1.06 g, yield 57percent, mp 183-186 °C). 1H NMR (DMSO-d6, 400 MHz): 13.16 (s, 2H, Hc), 9.06 (t, 4Jf-d = 1.6 Hz, 1H, Hf), 8.26 (dd, 4Jd-f = 1.6 Hz, 3Jd-e = 7.8 Hz, 2H, Hd), 7.74 (t, 3Je-d = 7.8 Hz, 1H, He), 7.69 (bs, 2H, Hb’), 7.58 (bs, 2H, Hb), 7.24 (d, 3Ja-b = 4.3 Hz, 4H, HaHa’). 13C NMR (DMSO-d6, 100 MHz): 125.3 (Cf), 128.0 (Cd), 130.2 (Ce), 119.5-112.1 (Cb), 123.3-122.4 (Ca). HRMS-ESI (m/z): calcd for [BBB+H]+ C20H15N4, 311.1291; found, 311.1294 (error: 1 ppm).Isophthalic acid (1.130 g, 6.8 mmol) and 1, 2-diaminobenzene (1.417 g, 13.1 mmol) were dissolved in 20 mL of polyphosphoric acid. The stirred mixture was maintained at 190 °C for 24 h. The solution was allowed to cool at room temperature (20 – 25 °C) and slowly stirred in 50 mL of ice. The reaction mixture was neutralized with NaOH and the precipitate was filtered out and washed with cold water. The solid was recrystallized from methanol to yield a white-off solid (1.06 g, yield 57percent, mp 183-186 °C). 1H NMR (DMSO-d6, 400 MHz): 13.16 (s, 2H, Hc), 9.06 (t, 4Jf-d = 1.6 Hz, 1H, Hf), 8.26 (dd, 4Jd-f = 1.6 Hz, 3Jd-e = 7.8 Hz, 2H, Hd), 7.74 (t, 3Je-d = 7.8 Hz, 1H, He), 7.69 (bs, 2H, Hb’), 7.58 (bs, 2H, Hb), 7.24 (d, 3Ja-b = 4.3 Hz, 4H, HaHa’). 13C NMR (DMSO-d6, 100 MHz): 125.3 (Cf), 128.0 (Cd), 130.2 (Ce), 119.5-112.1 (Cb), 123.3-122.4 (Ca). HRMS-ESI (m/z): calcd for [BBB+H]+ C20H15N4, 311.1291; found, 311.1294 (error: 1 ppm).

Computed Properties

Molecular Weight:310.4
XLogP3:4.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:310.121846464
Monoisotopic Mass:310.121846464
Topological Polar Surface Area:57.4
Heavy Atom Count:24
Complexity:403
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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