1981
DOI: 10.1107/s056774088100736x
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Structure of 4-homosulfanilamide hydrochloride

Abstract: STRUCTURE OF 4-HOMOSULFANILAMIDE HYDROCHLORIDEmolecules are stacked roughly parallel to the ab plane at average intervals of 3.9 A and there is a distinct overlap of the benzene rings in the z direction.

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Cited by 9 publications
(6 citation statements)
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“…The protonation on the one of the N sites is confirmed from C-N bond distance. The other geometrical parameters of the cation are in agreement with the reported structures of 4-homosulfanilamide hydrochloride (Chatterjee et al, 1981), 4aminobenzenesulfonamide (Gelbrich et al, 2008), bis(4-Aminosulfonyl)benzeneammonium hexafluorosilicate (Gelmboldt et al,2004), 4-sulfonamidoanilinium 3,5-dinitrosalicylate (Smith et al, 2001) and 4-sulfamoylanilinium chloride (Zaouali Zgolli et al, 2010).…”
Section: S1 Commentsupporting
confidence: 87%
See 1 more Smart Citation
“…The protonation on the one of the N sites is confirmed from C-N bond distance. The other geometrical parameters of the cation are in agreement with the reported structures of 4-homosulfanilamide hydrochloride (Chatterjee et al, 1981), 4aminobenzenesulfonamide (Gelbrich et al, 2008), bis(4-Aminosulfonyl)benzeneammonium hexafluorosilicate (Gelmboldt et al,2004), 4-sulfonamidoanilinium 3,5-dinitrosalicylate (Smith et al, 2001) and 4-sulfamoylanilinium chloride (Zaouali Zgolli et al, 2010).…”
Section: S1 Commentsupporting
confidence: 87%
“…For the biological importance of the title compound, see: Kent (2000). For related structures, see: Allé aume & Decap (1965a,b); Buttle et al (1936); Chatterjee et al (1981); Gelbrich et al (2007Gelbrich et al ( , 2008; Gelmboldt et al (2004); Hughes et al (1999);O'Connell & Maslen (1967); O'Connor & Maslen (1965); Smith et al (2001);Zaouali Zgolli et al (2010). For the polymorphism of sulfanilamide, see: Burger (1973).…”
Section: Related Literaturementioning
confidence: 99%
“…The S-N and N-C bonds are amongst the shortest when compared with the values in related compounds (Shefter, Chmielewicz, Blount, Brennan, Sackman & Sackman, 1972;Chatterjee, Dattagupta & Saha, 1981, 1982 while the S-C and S-O bonds are amongst the longest of those observed in related compounds. The endocyclic angle at C(27) is 121.9 (3) °, and is within the normal range observed in sulfonamides with a pyrimidine ring.…”
mentioning
confidence: 88%
“…Those who then effectively used the data included R. Srinivasan of the Madras University 32,33 , to start with, among others [34][35][36][37] . Substantial progress was made during this phase in the crystallography of amino acids and peptides [38][39][40][41][42][43] , including the relevance of their supramolecular association to chemical evolution and origin of life 44 , nucleic acids and their constituents 45 , ionophores and related compounds 46,47 , and medicinally important molecules [48][49][50] . The same is true about NMR studies on medium-sized biomolecules [51][52][53] .…”
Section: The Immediate Aftermathmentioning
confidence: 99%