A41208

2-Aminobenzophenone

Name: 2-Aminobenzophenone
Brand: ALDRICH
Price: 28.5 USD
Availability: InStock

98%

Synonym(s):

2-Aminophenyl phenyl ketone, 2-Benzoylaniline

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About This Item

Linear Formula:

H₂NC₆H₄C(O)C₆H₅

CAS Number:

2835-77-0

Molecular Weight:

197.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24890744

EC Number:

220-613-9

Beilstein/REAXYS Number:

743425

MDL number:

MFCD00007713

Key Documents

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Product Name

2-Aminobenzophenone, 98%

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

SMILES string

Nc1ccccc1C(=O)c2ccccc2

assay

98%

form

crystals

mp

103-107 °C (lit.)

Quality Level

100

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Show Differences

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This Item	748439	A45564	A41402
Sigma-Aldrich A41208 2-Aminobenzophenone	Sigma-Aldrich 748439 2-Aminobenzhydrol	Sigma-Aldrich A45564 2-Amino-5-chlorobenzophenone	Sigma-Aldrich A41402 4-Aminobenzophenone
assay 98%	assay 97%	assay 98%	assay -
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 200
form crystals	form solid	form powder	form powder
mp 103-107 °C (lit.)	mp 113-118 °C	mp 96-98 °C (lit.)	mp 121-124 °C (lit.)

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Colon-targeted delivery of solubilized bisacodyl by doubly enteric-coated multiple-unit tablet.

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

Effects of conformational restriction of 2-amino-3-benzoylthiophenes on A(1) adenosine receptor modulation.

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.

2-(4-Ethoxy phenyl)-4-phenyl quinoline organic phosphor for solution processed blue organic light-emitting diodes.

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

Synthesis and properties of quinazoline-based versatile exciplex-forming compounds.

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

B-ring-aryl substituted luotonin A analogues with a new binding mode to the topoisomerase 1-DNA complex show enhanced cytotoxic activity.

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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2-Aminobenzophenone