Results 41 to 50 of about 16,265 (239)

N-(3-Chlorophenyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
The conformation of the N-H bond in the structure of the title compound (N3CPBA), C(13)H(10)ClNO, is anti to the meta chloro substituent in the aniline benzene ring, similar to that observed with respect to the ortho chloro substituent in N-(2-chloro-phen-yl)benzamide (N2CPBA) and meta chloro substituent in N-(3,4-dichloro-phen-yl)benzamide (N34DCPBA),
Hartmut Fuess   +4 more
openaire   +3 more sources

N-(4-Methylphenyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2007
The structure of the title compound, C(14)H(13)NO, resembles those of N-(2-chloro-phen-yl)benzamide, 2-chloro-N-phenyl-benzamide, N-(2,3-dichloro-phen-yl)benzamide, N-(3,4-dichloro-phen-yl)benzamide and 2-chloro-N-(2-chloro-phen-yl)benzamide with similar bond parameters.
B. Thimme Gowda   +3 more
openaire   +3 more sources

Synthesis, Spectroscopic Properties and Antipathogenic Activity of New Thiourea Derivatives

open access: yesMolecules, 2011
A number of acylthioureas, 2-((4-methylphenoxy)methyl)-N-(aryl-carbamothioyl)benzamides (aryl = 3,5-dichlorophenyl, 2,3-dichlorophenyl, 3,4-dichloro-phenyl, 2,4,5-trichlorophenyl, 3,4,5-trichlorophenyl, 2-bromophenyl, 2,4-dibromophenyl, 2,5-dibromophenyl,
Carmen Limban   +2 more
doaj   +1 more source

N-(2-Nitrophenyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2009
In the title compound, C(13)H(10)N(2)O(3), the central C-C(=O)-N-C amide unit makes dihedral angles of 21.68 (4) and 19.08 (4)°, respectively, with the phenyl and nitro-benzene rings. The two aromatic rings are inclined at 3.74 (3)° and the nitro group is skewed out of the attached benzene ring plane by 18.55 (8)°. An intra-molecular N-H⋯O inter-action
Aamer Saeed, Jim Simpson
openaire   +3 more sources

The PIFA-initiated oxidative cyclization of 2-(3-butenyl)quinazolin-4(3H)-ones – an efficient approach to 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones

open access: yesBeilstein Journal of Organic Chemistry, 2021
A regioselective method for the synthesis of 1-(hydroxymethyl)-2,3-dihydropyrrolo[1,2-a]quinazolin-5(1H)-ones – close structural analogs of naturally occurring vasicinone alkaloids – is described.
Alla I. Vaskevych   +5 more
doaj   +1 more source

N-(3-Methylphenyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
The asymmetric unit of the title compound, C(14)H(13)NO, contains four mol-ecules, which are linked through N-H⋯O hydrogen bonds into two symmetry-independent chains running parallel to [001] and [101]. The N-H and C=O bonds of the amide groups are trans oriented in all four mol-ecules.
B. Thimme Gowda   +3 more
openaire   +3 more sources

2-Hydroxy-N-phenylbenzamides and Their Esters Inhibit Acetylcholinesterase and Butyrylcholinesterase

open access: yesBiomolecules, 2019
The development of novel inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) represents a viable approach to alleviate Alzheimer’s disease.
Martin Krátký   +5 more
doaj   +1 more source

Antiviral Mechanisms of N-Phenyl Benzamides on Coxsackie Virus A9

open access: yesPharmaceutics, 2023
Enteroviruses are one of the most abundant groups of viruses infecting humans, and yet there are no approved antivirals against them. To find effective antiviral compounds against enterovirus B group viruses, an in-house chemical library was screened ...
Mira Laajala   +7 more
doaj   +1 more source

N-(3,5-Dimethoxyphenyl)benzamide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2011
The title compound, C(15)H(15)NO(3), was prepared by stirring benzoyl chloride with 3,5-dimeth-oxy-aniline in dioxane at ambient temperature. The dimeth-oxy-phen-yl-amide segment of the mol-ecule is almost planar, with a C-N-C=O torsion angle of -4.1 (4)°. The two benzene rings are inclined at an angle of 76.66 (13)°.
Hong-Lei Li, Jiang-Tao Cui
openaire   +3 more sources

Cobalt-Promoted Dimerization of Aminoquinoline Benzamides

open access: yes, 2016
A method for aminoquinoline-directed, cobalt-promoted dimerization of benzamides has been developed. Reactions proceed in ethanol solvent in the presence of Mn­(OAc)2 cocatalyst and Na2CO3 base and use oxygen as a terminal oxidant.
Liene Grigorjeva (1332981)   +1 more
core   +1 more source

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