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A41208

2-Aminobenzophenone

Name: 2-Aminobenzophenone
Brand: ALDRICH

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

Assay:

98%

Form:

crystals

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Properties

Quality Level

100

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

Description

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

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

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.

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Global Trade Item Number

SKU	GTIN
A41208-25G	04061832492056
A41208-5G	04061832492063