1-Methyl-3-phenylthiourea
2014 ◽
Vol 70
(5)
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pp. o528-o528
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The title compound, C8H10N2S, was prepared by reaction of methylamine solution, KOH and phenyl-isothiocyanate in ethanol. It adopts asyn-Me andanti-Ph conformation relative to the C=S double bond. The dihedral angle between the N—C(=S)—N thiourea and phenyl planes is 67.83 (6)°. In the crystal, the molecules centrosymmetrical dimers by pairs of N(Ph)—H...S hydrogen bonds. The dimers are linked by N(Me)—H...S hydrogen bonds into layers parallel to (100).
2012 ◽
Vol 68
(4)
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pp. o1002-o1002
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2019 ◽
Vol 75
(5)
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pp. 571-575
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2006 ◽
Vol 62
(7)
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pp. o2687-o2688
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2006 ◽
Vol 62
(7)
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pp. o2685-o2686
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2012 ◽
Vol 68
(6)
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pp. o1819-o1819
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2014 ◽
Vol 70
(7)
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pp. o751-o751
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