255254
3-Aminobenzophenone
97%
Synonym(s):
3-Benzoylaniline
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About This Item
Linear Formula:
H2NC6H4C(O)C6H5
CAS Number:
Molecular Weight:
197.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
81-84 °C (lit.)
SMILES string
Nc1cccc(c1)C(=O)c2ccccc2
InChI
1S/C13H11NO/c14-12-8-4-7-11(9-12)13(15)10-5-2-1-3-6-10/h1-9H,14H2
InChI key
FUADXEJBHCKVBN-UHFFFAOYSA-N
General description
3-Aminobenzophenone forms cyclodextrin (α and β) based nanostructures through the supramolecular self assembly.
Application
3-Aminobenzophenone has been used in the synthesis of racemic benzophenone ureas, chiral photoaffinity labeling probes.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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N Rajendiran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 127, 52-60 (2014-03-19)
Cyclodextrin (α and β) based nanostructures formed with 2-aminobenzophenone, 3-aminobenzophenone through the supramolecular self assembly are studied by absorption, fluorescence, time-resolved fluorescence, SEM, TEM, FT-IR, DSC, PXRD and (1)H NMR. The unequal layer by layer nanosheets and nanoribbons are formed
Elizabeth M Hadac et al.
Journal of medicinal chemistry, 49(3), 850-863 (2006-02-03)
An understanding of the molecular basis of drug action provides opportunities for refinement of drug properties and for development of more potent and selective molecules that act at the same biological target. In this work, we have identified the active
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