Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Aromatic ketones >  3,4-Dimethylbenzophenone

3,4-Dimethylbenzophenone

Basic information Safety Supplier Related

3,4-Dimethylbenzophenone Basic information

Product Name:
3,4-Dimethylbenzophenone
Synonyms:
  • Benzophenone, 3,4-dimethyl-
  • Methanone, (3,4-dimethylphenyl)phenyl-
  • 3,4-DIMETHYLBENZOPHENONE
  • (3,4-Dimethylphenyl)phenyl-methanone
  • (3,4-Dimethylphenyl)phenyl ketone
  • Phenyl 3,4-xylyl ketone
  • 3,4-Dimethylbenzophe
  • 3,4-Dimethylb
CAS:
2571-39-3
MF:
C15H14O
MW:
210.27
EINECS:
219-916-9
Product Categories:
  • Polymerization Initiators
  • Aromatic Benzophenones & Derivatives (substituted)
  • Benzophenone
  • Organic Photoinitiators
Mol File:
2571-39-3.mol
More
Less

3,4-Dimethylbenzophenone Chemical Properties

Melting point:
45-47 °C (lit.)
Boiling point:
335°C
Density 
1.0232 (rough estimate)
refractive index 
1.5361 (estimate)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Light yellow
BRN 
1952043
InChI
InChI=1S/C15H14O/c1-11-8-9-14(10-12(11)2)15(16)13-6-4-3-5-7-13/h3-10H,1-2H3
InChIKey
JENOLWCGNVWTJN-UHFFFAOYSA-N
SMILES
C(C1=CC=C(C)C(C)=C1)(C1=CC=CC=C1)=O
CAS DataBase Reference
2571-39-3(CAS DataBase Reference)
NIST Chemistry Reference
3,4-Dimethylbenzophenone(2571-39-3)
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-24/25-22-36
WGK Germany 
3
HS Code 
29143990

MSDS

More
Less

3,4-Dimethylbenzophenone Usage And Synthesis

Description

3,4-Dimethylbenzophenone is an important chemical material for organic synthesis or laboratory research.

Synthesis

65614-94-0

2571-39-3

The general procedure for the synthesis of 3,4-dimethylbenzophenone from the compound (CAS: 65614-94-0) was carried out as follows: a magnetic stirrer was added to a Schlenk tube which had been pre-dried in an oven, and 1,2-diarylalkyn-1 (0.5 mmol), aniline (0.6 mmol), K2CO3 (0.5 mmol) and Cu(OAc)2 (0.075 mmol). Subsequently, DMSO (3 mL) was added as solvent, the reaction tube was sealed and purged by passing oxygen through a syringe. The reaction mixture was placed in an oil bath at 120 °C and the reaction was continuously stirred for 16-18 hours. Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate (30 mL) and filtered through a diatomaceous earth pad. The organic phase was collected and washed sequentially with saturated NaCl solution (8 mL), saturated NH4Cl solution (8 mL) and again saturated NaCl solution (8 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent to obtain the crude product. Finally, the crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate gradient) to obtain the target compound 3,4-dimethylbenzophenone.

References

[1] RSC Advances, 2015, vol. 5, # 1, p. 690 - 693
[2] Tetrahedron, 2015, vol. 71, # 7, p. 1045 - 1049

3,4-DimethylbenzophenoneSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com