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4,4'-Dichlorobenzophenone

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Identification
Molecular formula
C13H8Cl2O
CAS number
90-98-2
IUPAC name
bis(4-chlorophenyl)methanone
State
State

At room temperature, 4,4'-Dichlorobenzophenone is typically in a solid state. It consists of crystalline particles that can be visibly seen and handled.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
253.11g/mol
Molar mass
253.1380g/mol
Density
1.3130g/cm3
Appearence

4,4'-Dichlorobenzophenone appears as a white to pale yellow crystalline solid. It may exhibit a slightly different hue depending on the purity and specific sample preparation.

Comment on solubility

Solubility of bis(4-chlorophenyl)methanone

Bis(4-chlorophenyl)methanone, also known as dibenzoyl, exhibits distinctive solubility properties that reflect its chemical structure. Understanding its solubility can be quite important for applications in various fields, including organic synthesis and pharmaceuticals.

The solubility of bis(4-chlorophenyl)methanone can be characterized as follows:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol, acetone, and chloroform.
  • Water Solubility: It has poor solubility in water, which limits its use in aqueous environments.
  • Temperature Dependence: Solubility can increase with temperature; thus, heating organic solvents can enhance the dissolution of this compound.

Furthermore, as stated in chemical literature, "the solubility in organic media is often crucial for effective reactivity and the performance of the compound in synthetic applications." Therefore, when working with bis(4-chlorophenyl)methanone, it is essential to consider the choice of solvent, taking into account its solubility profile to achieve optimal results.

Interesting facts

Interesting Facts about Bis(4-chlorophenyl)methanone

Bis(4-chlorophenyl)methanone, also known for its role in various chemical reactions and applications, is an intriguing compound within organic chemistry. Here are some key points that highlight its significance:

  • Structural Significance: This compound features two 4-chlorophenyl groups attached to a central carbonyl group. This unique structure contributes to its reactivity and stability compared to similar compounds.
  • Applications in Synthesis: Bis(4-chlorophenyl)methanone is often utilized in synthetic organic chemistry as an intermediate. It can be employed in the manufacturing of numerous pharmaceuticals and agrochemicals, showcasing its utility in the development of useful chemical products.
  • Biological Activity: Research indicates that derivatives of bis(4-chlorophenyl)methanone may exhibit interesting biological activity. This has opened pathways for further investigation into its potential therapeutic applications, particularly in the field of medicinal chemistry.
  • Research and Development: Ongoing studies aim to explore more fully the reactivity of bis(4-chlorophenyl)methanone in various chemical processes. Its mechanism of action and behavior in different conditions are areas of active investigation among chemists.
  • Environmental Awareness: Like many chlorinated compounds, it’s important to approach bis(4-chlorophenyl)methanone with an understanding of its environmental impact. Researchers are looking into safer alternatives while also studying its degradation pathways in the environment.

As a compound featuring both aromatic and carbonyl functions, bis(4-chlorophenyl)methanone represents a fascinating area of study in organic synthesis and medicinal chemistry. Keep an eye on future developments, as this compound may very well contribute to significant advancements in chemical science!

Synonyms
4,4'-Dichlorobenzophenone
90-98-2
Bis(4-chlorophenyl)methanone
Methanone, bis(4-chlorophenyl)-
DCBP
Bis(4-chlorophenyl) ketone
Di(p-chlorophenyl)ketone
4,4-DICHLOROBENZOPHENONE
Di(4-chlorophenyl)ketone
Bis(p-chlorophenyl)ketone
p-Dichlorobenzophenone
Benzophenone, 4,4'-dichloro-
USAF DO-4
P,P'-DICHLOROBENZOPHENONE
Bis(4-chlorophenyl)ketone
NSC 8787
MFCD00000623
UNII-3MTL0YC2Q5
EINECS 202-030-1
3MTL0YC2Q5
BRN 0643345
DTXSID3037626
AI3-03064
p,p-Dichlorobenzophenone
4,4'-Dichlorobenzophenone (DBP)
4,4'-DBP
NSC-8787
DTXCID1017626
4-07-00-01376 (Beilstein Handbook Reference)
DBP (VAN)
4,4'-dichloro-benzophenone
4,4 inverted exclamation mark -dichlorobenzophenone
Di(pchlorophenyl)ketone
Di(4chlorophenyl)ketone
p,p'dichlorobenzophenone
Bis(pchlorophenyl)ketone
Bis(4chlorophenyl)ketone
4-4-Dichlorobenzophenone
Bis(4chlorophenyl) ketone
WLN: GR DVR DG
4,4;-dichlorobenzophenone
bmse000517
4,4\'-Dichlorobenzophenone
Benzophenone, 4,4'dichloro
SCHEMBL51827
bis(4-chlorophenyl)-methanone
Methanone, bis(4chlorophenyl)
4,4'-Dichlorobenzophenone 10 microg/mL in Cyclohexane
Bis(4-chlorophenyl)methanone #
CHEMBL1870191
bis-(4-chloro-phenyl)-methanone
NSC8787
CHEBI:194706
4,4'-Dichlorobenzophenone, 99%
Tox21_302130
STK290986
AKOS000282714
CS-W012634
HY-W011918
CAS-90-98-2
NCGC00163933-01
NCGC00255637-01
AC-10278
AS-11851
SY009660
DB-057234
D1621
NS00008814
EN300-31834
4,4'-DBP, PESTANAL(R), analytical standard
A10286
C06643
AE-641/00433006
4,4'-Dichlorobenzophenone, purum, >=99.0% (GC)
Q4637048
Z335453234
202-030-1