A monoclinic modification of 2-[(1,3-benzothiazol-2-yl)iminomethyl]phenol

Abdullah Mohamed Asiri; Salman A. Khan; Kong Wai Tan; Seik Weng Ng

doi:10.1107/s1600536810023755

Abstract

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In the title Schiff base, C(14)H(10)N(2)OS, the azomethine double bond is in an E configuration; the benzothiazolyl ring (r.m.s. deviation = 0.007 Å) is coplanar with the phenyl-ene ring (r.m.s. deviation = 0.007 Å), the two rings being slightly bent at 2.6 (1)°. The hy-droxy H atom forms an intra-molecular hydrogen bond to the imino group. The bond dimensions of the monoclinic modification are similar to those of the ortho-rhom-bic modification [Liu et al. (2009 ▶). Acta Cryst. E65, o738].

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A monoclinic modification of 2-[(1,3-benzothiazol-2-yl)iminomethyl]phenol

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