Results 71 to 80 of about 33,916 (231)

Benzamide–picric acid (1/1) [PDF]

Acta Crystallographica Section E Structure Reports Online, 2010
In the title compound, C(7)H(7)NO·C(6)H(3)N(3)O(7), one of the nitro groups of the picric acid mol-ecule lies in the plane of the attached benzene ring [dihedral angle = 1.4 (1)°] while the other two are twisted away by 9.9 (1) and 30.3 (1)°. In the benzamide mol-ecule, the amide group is almost coplanar with the benzene ring [dihedral angle = 4.4 (1)°]
Sivaramkumar, M. S., Velmurugan, R., Sekar, M., Ramesh, P., Ponnuswamy, M. N.   +4 more
openaire   +2 more sources

Crystal structure of 2-(1,3,7,9-tetramethyl-2,4,6,8-tetraoxo-1,2,3,4,6,7,8,9-octahydropyrido[2,3-d:6,5-d′]dipyrimidin-5-yl)benzamide dimethylformamide hemisolvate

Acta Crystallographica Section E, 2014
The title compound, C20H18N6O5·0.5C3H7NO, crystallized as a dimethylformamide (DMF) solvate. In the main molecule, the dihedral angle between the pyridodipyrimidine fused-ring system and the benzamide substituent is 82.26 (11)°.
Armen Ayvazyan
doaj   +1 more source

Ab-initio crystal structure analysis and refinement approaches of oligo p-benzamides based on electron diffraction data [PDF]

, 2012
Ab-initio crystal structure analysis of organic materials from electron diffraction data is presented. The data were collected using the automated electron diffraction tomography (ADT) technique.
Brunklaus, Gunther, Gorelik, Tatiana E., Kilbinger, Andreas F. M., Kolb, Ute, Streek, Jacco van de   +4 more
core   +1 more source

2-Anilino-N-methyl-N-phenylbenzamide

Acta Crystallographica Section E, 2009
The title compound, C20H18N2O, is composed of three aromatic rings, the dihedral angles between the phenyl and benzamide rings, and between the benzamide and aniline rings being 59.86 (9) and 46.57 (10)°, respectively.
Da-Bin Qin, Chenglin Zhou, Xing-Xing Yang   +2 more
doaj   +1 more source

A chemoselective and continuous synthesis of m-sulfamoylbenzamide analogues [PDF]

, 2017
For the synthesis of m-sulfamoylbenzamide analogues, small molecules which are known for their bioactivity, a chemoselective procedure has been developed starting from m-(chlorosulfonyl) benzoyl chloride.
Heugebaert, Thomas, Kerchev, Pavel, Stevens, Christian, Van Breusegem, Frank, van der Meer, Tom, Verlee, Arno   +5 more
core   +3 more sources

2-Bromo-N-(dibenzylcarbamothioyl)benzamide [PDF]

Acta Crystallographica Section E Structure Reports Online, 2011
The 2-bromo-benzoyl group in the title compound, C(22)H(19)BrN(2)OS, adopts an E conformation with respect to the thiono S atom across the N-C bond. In the crystal structure, the mol-ecule is stablized by N-H⋯O inter-molecular hydrogen bonds, forming a one-dimensional chain along the b axis.
Mohd Faizal Md Nasir, Ibrahim N. Hassan, Wan Ramli Wan Daud, Bohari M. Yamin, Mohammad B. Kassim   +4 more
openaire   +3 more sources

Novas N-benzoiltiraminas de Swinglea glutinosa (Rutaceae)

Química Nova, 2012
Phytochemical studies of the leaves and fruits have led to the identification of the known amides (E)-N-methyl-cinnamamide, N-benzoyltyramine, N-benzoyl-O-geranyltyramine, N-benzoyl-O-(4-acetoxyl)-geranyltyramine, in addition to the new N-{2-[4-(butoxyl ...
Cristovam do Nascimento Cerqueira, Djalma A. P. dos Santos, Karla da Silva Malaquias, Murilo Marinho de Castro Lima, Maria Fátima das Graças Fernandes da Silva, João Batista Fernandes, Paulo Cezar Vieira   +6 more
doaj   +1 more source

Switching polymorph stabilities with impurities provides a thermodynamic route to benzamide form III

Communications Chemistry, 2021
The formation of solid solutions can result in changes of relative stabilities of crystal polymorphs. Here, the elusive form III of benzamide is stabilized through solid solution formation with nicotinamide.
Weronika Kras, Andrea Carletta, Riccardo Montis, Rachel A. Sullivan, Aurora J. Cruz-Cabeza   +4 more
doaj   +1 more source

Genetic code expansion for chemosensing and chemical actuation of biological functions

Bulletin of the Korean Chemical Society, EarlyView.
Genetic code expansion (GCE) broadens the chemical repertoire for precise control of protein function in biological systems. This review highlights GCE‐based sensing and actuating systems that operate through selective interactions between noncanonical amino acids and chemical triggers.
Jieun Bae, Dong‐Hyun Kim, Minseob Koh
wiley   +1 more source

5-Amino-2-chloro-4-fluoro-N-(N-isopropyl-N-methylsulfamoyl) benzamide, C11H15O3ClFN3S

Zeitschrift für Kristallographie - New Crystal Structures, 2023
C11H15O3ClFN3S, triclinic, P1‾ $P\overline{1}$ (no. 2), a = 7.8107(11) Å, b = 9.1644(13) Å, c = 11.3521(15) Å, α = 67.543(2)°, β = 72.776(2)∘ $72.776{(2)}^{\circ }$ , γ = 88.529(2)∘ $88.529{(2)}^{\circ }$ , V = 713.76(17) Å3, Z = 2, Rgt ${R}_{\mathit{g}\
Jie Wang, Xiao Shu-Zhen, Cong Huang, Liu Ya-Qiang, Peng Da-Yong   +4 more
doaj   +1 more source