Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

225274

Sigma-Aldrich

4,4′-Dimethylbenzophenone

99%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(CH3C6H4)2CO
CAS Number:
611-97-2
Molecular Weight:
210.27
Beilstein:
1240527
EC Number:
210-287-6
MDL number:
MFCD00017214
UNSPSC Code:
12352100
PubChem Substance ID:
24853487
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

bp

200 °C/17 mmHg (lit.)

mp

90-93 °C (lit.)

functional group

ketone

SMILES string

Cc1ccc(cc1)C(=O)c2ccc(C)cc2

InChI

1S/C15H14O/c1-11-3-7-13(8-4-11)15(16)14-9-5-12(2)6-10-14/h3-10H,1-2H3

InChI key

ZWPWLKXZYNXATK-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

4,4′-Dimethylbenzophenone reacts with bis(trichlorotitanium phenoxide), a bidentate Lewis acid, to form a crystalline complex.

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
STBL0493
STBJ8955
S15363V
S15363
01804HH

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

Okba Saied et al.
Inorganic chemistry, 37(11), 2620-2625 (2001-10-24)
Treatment of 2,7-bis(1,1-dimethylethyl)fluorene-1,8-diol (3) with 2 equiv of TiCl(4) converts the two OH groups into OTiCl(3) groups and thereby yields bis(trichlorotitanium phenoxide) 7, a structurally well-defined reagent that holds two sites of strong Lewis acidity in close proximity. Bidentate Lewis

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