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A41208

Sigma-Aldrich

2-Aminobenzophenone

98%

Sinónimos:

2-Aminophenyl phenyl ketone, 2-Benzoylaniline

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About This Item

Fórmula lineal:
H2NC6H4C(O)C6H5
Número de CAS:
2835-77-0
Peso molecular:
197.23
Beilstein/REAXYS Number:
743425
EC Number:
220-613-9
MDL number:
MFCD00007713
UNSPSC Code:
12352100
PubChem Substance ID:
24890744
NACRES:
NA.22

assay

98%

form

crystals

mp

103-107 °C (lit.)

SMILES string

Nc1ccccc1C(=O)c2ccccc2

InChI

1S/C13H11NO/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-9H,14H2

InChI key

MAOBFOXLCJIFLV-UHFFFAOYSA-N

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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Hee J Park et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 102, 172-179 (2017-03-11)
A doubly enteric-coated multiple-unit tablet (DET) of bisacodyl (BD) was formulated to selectively deliver the stimulant laxative to the large intestine. Solubilized BD in surfactants was adsorbed into the porous carrier and primarily coated with different combinations of pH-sensitive polymers
Minakshi Ghate et al.
Luminescence : the journal of biological and chemical luminescence, 33(6), 999-1009 (2018-06-01)
This paper reports the synthesis and characterization of 2-(4-ethoxyphenyl)-4-phenyl quinoline (OEt-DPQ) organic phosphor using an acid-catalyzed Friedlander reaction and the preparation of blended thin films by molecularly doping OEt-DPQ in poly(methyl methacrylate) (PMMA) at different wt%. The molecular structure of
Luigi Aurelio et al.
Journal of medicinal chemistry, 53(18), 6550-6559 (2010-09-03)
2-Amino-3-benzoylthiophenes (2A3BTs) have been widely reported to act as allosteric enhancers (AEs) at the A(1) adenosine receptor (A(1)AR). Herein we describe the synthesis of a series of 1-aminoindeno[1,2-c]thiophen-8-ones and a series of (2-aminoindeno[2,1-b]thiophen-3-yl)(phenyl)methanones as conformationally rigid analogues of the 2A3BTs.
Rasa Keruckiene et al.
Beilstein journal of organic chemistry, 16, 1142-1153 (2020-06-20)
Three compounds, bearing a quinazoline unit as the acceptor core and carbazole, dimethyldihydroacridine, or phenothiazine donor moieties, were designed and synthesized in two steps including a facile copper-catalyzed cyclization and a nucleophilic aromatic substitution reaction. The photophysical properties of the
Víctor González-Ruiz et al.
PloS one, 9(5), e95998-e95998 (2014-05-17)
Topoisomerase 1 inhibition is an important strategy in targeted cancer chemotherapy. The drugs currently in use acting on this enzyme belong to the family of the camptothecins, and suffer severe limitations because of their low stability, which is associated with
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