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Sigma-Aldrich

3-Aminobenzophenone

97%

Synonym(s):

3-Benzoylaniline

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About This Item

Linear Formula:
H2NC6H4C(O)C6H5
CAS Number:
2835-78-1
Molecular Weight:
197.23
EC Number:
220-614-4
MDL number:
MFCD00017103
UNSPSC Code:
12352100
PubChem Substance ID:
24855409
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

81-84 °C (lit.)

functional group

ketone
phenyl

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCH1567
MKBZ9981V
MKBW5039V
MKBT3660V
04812DD

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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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