4,4'-Dichlorobenzophenone

Product Information

Molecular Formula:
C13H8Cl2O
Molecular Weight:
251.11
Description
4,4'-Dichlorobenzophenone has antiviral and antifungal abilities and plays a key role in formulating drugs against a range of viral and fungal diseases.
Synonyms
Methanone, bis(4-chlorophenyl)-; Benzophenone, 4,4'-dichloro-; 4,4'-DCBP; Bis(4-chlorophenyl) ketone; Bis(p-chlorophenyl) ketone; DBP; DBP (degradation product); DCBP; DCBP (ketone); Di(4-chlorophenyl) ketone; Di(p-chlorophenyl) ketone; NSC 8787; p,p'-Dichlorobenzophenone
IUPAC Name
bis(4-chlorophenyl)methanone
Canonical SMILES
C1=CC(=CC=C1C(=O)C2=CC=C(C=C2)Cl)Cl
InChI
InChI=1S/C13H8Cl2O/c14-11-5-1-9(2-6-11)13(16)10-3-7-12(15)8-4-10/h1-8H
InChI Key
OKISUZLXOYGIFP-UHFFFAOYSA-N
Boiling Point
353°C
Melting Point
147.5°C
Purity
≥95%
Density
1.311±0.06 g/cm3
Solubility
Soluble in hot Acetone
Appearance
White to Light Yellow Powder to Crystal
Storage
Store at RT
LogP
4.22440

Safety Information

Precautionary Statement
P264, P270, P301+P312, P330, and P501
Signal Word
Warning

Computed Properties

XLogP3
4.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
2
Exact Mass
249.9952203 g/mol
Monoisotopic Mass
249.9952203 g/mol
Topological Polar Surface Area
17.1Ų
Heavy Atom Count
16
Formal Charge
0
Complexity
214
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114130212-A Method for preparing separation membrane by using small molecule monomer 2021-11-30
JP-2022031758-A A photosensitive resin composition, a photosensitive film using the photosensitive resin composition, a method for forming a resist pattern, and a printed wiring board. 2021-11-19
CN-113881041-A Method for large-scale preparation of high-crystallization high-specific-surface-area covalent triazine framework 2021-11-18
CN-113912778-A Insulating material for high-voltage cable, preparation method and preparation base material thereof 2021-10-21
CN-113754667-A Method for rapidly and massively preparing high-crystalline semiconductor covalent triazine framework 2021-09-28
CN-113829642-A Hollow surface fabric seal and forming die and method thereof 2021-09-17
CN-113637642-A Hybridoma cell strain capable of secreting monoclonal antibody of dicofol and application of hybridoma cell strain 2021-09-16
CN-113667123-A Polyarylene sulfide compound with ultraviolet fluorescent tracing function and preparation method thereof 2021-09-10
CN-113735754-A Preparation method of high-purity powdery di (2, 4-dichlorobenzoyl) peroxide 2021-08-20
CN-113736260-A Vibrating diaphragm for sound production device and sound production device 2021-08-16

Literatures

PMID Publication Date Title Journal
21291947 2011-04-11 Dicofol degradation to p,p'-dichlorobenzophenone - a potential antiandrogen Toxicology
21300395 2011-03-01 Determination of n-octanol/water partition coefficient for DDT-related compounds by RP-HPLC with a novel dual-point retention time correction Chemosphere
20979383 2010-11-24 Simultaneous degradation of mixed insecticides by mixed fungal culture isolated from sewage sludge Journal of agricultural and food chemistry
19846197 2010-01-01 Anaerobic biodegradation of organochlorine pesticides in contaminated soil - significance of temperature and availability Chemosphere
20390935 2010-01-01 Bioremediation of chlorinated pesticide-contaminated soil using anaerobic sludges and surfactant addition Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes
18942076 2009-02-01 Electronic structure and biological activity of chosen DDT-type insecticides studied by 35Cl-NQR Magnetic resonance in chemistry : MRC
18247497 2008-03-06 On the role of samarium/HMPA in the post electron-transfer steps in SmI2 reductions Organic letters
18023468 2008-03-01 Pesticides removal in the process of drinking water production Chemosphere
17960931 2007-11-15 Experimental and computational studies on the molecular energetics of chlorobenzophenones The journal of physical chemistry. B
16710056 2006-06-01 On the mechanism of some first-order enantiotropic solid-state phase transitions: from Simon through Ubbelohde to Mnyukh Acta crystallographica. Section B, Structural science
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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