5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone

Zhaoyang Li; Osamu Sato

doi:10.1107/S1600536813008787

5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone

Zhaoyang Li, Osamu Sato

Department of Fundamental Organic Chemistry

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

In the title Schiff base compound, C₁₀H₁₂BrN ₃OS, the C - N - N - C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers.

Original language	English
Pages (from-to)	o762
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	69
Issue number	5
DOIs	https://doi.org/10.1107/S1600536813008787
Publication status	Published - May 2013

All Science Journal Classification (ASJC) codes

Chemistry(all)
Materials Science(all)
Condensed Matter Physics

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10.1107/S1600536813008787

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title = "5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone",

abstract = "In the title Schiff base compound, C10H12BrN 3OS, the C - N - N - C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers.",

author = "Zhaoyang Li and Osamu Sato",

year = "2013",

month = may,

doi = "10.1107/S1600536813008787",

language = "English",

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pages = "o762",

journal = "Acta Crystallographica Section E: Structure Reports Online",

issn = "1600-5368",

publisher = "International Union of Crystallography",

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T1 - 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone

AU - Li, Zhaoyang

AU - Sato, Osamu

PY - 2013/5

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N2 - In the title Schiff base compound, C10H12BrN 3OS, the C - N - N - C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers.

AB - In the title Schiff base compound, C10H12BrN 3OS, the C - N - N - C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers.

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JF - Acta Crystallographica Section E: Structure Reports Online

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ER -

5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone

Abstract

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