Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

255254

Sigma-Aldrich

3-Aminobenzophenone

97%

Synonym(s):

3-Benzoylaniline

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCH1567
MKBZ9981V
MKBW5039V
MKBT3660V
04812DD

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

3′-Aminoacetophenone 97%

Sigma-Aldrich

139351

3′-Aminoacetophenone

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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service