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3,4-dichloroisochromen-1-one

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Identification
Molecular formula
C9H4Cl2O2
CAS number
31210-90-9
IUPAC name
3,4-dichloroisochromen-1-one
State
State

At room temperature, 3,4-dichloroisochromen-1-one is found in the solid state.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.00
Boiling point (Celsius)
333.00
Boiling point (Kelvin)
606.00
General information
Molecular weight
229.04g/mol
Molar mass
229.0380g/mol
Density
1.5600g/cm3
Appearence

3,4-Dichloroisochromen-1-one is a solid compound that typically appears as a crystalline powder. The color may vary slightly but it generally appears white or off-white.

Comment on solubility

Solubility of 3,4-Dichloroisochromen-1-one

The solubility of 3,4-dichloroisochromen-1-one (C9H4Cl2O2) is an intriguing aspect to consider. This compound exhibits unique properties due to its structure, influencing its solubility in various solvents.

Solubility Characteristics

3,4-Dichloroisochromen-1-one is generally poorly soluble in water, which is typical for many halogenated compounds. Here are some key points regarding its solubility:

  • Polar Solvents: This compound may show limited solubility in polar solvents such as ethanol or methanol.
  • Non-Polar Solvents: It tends to dissolve more readily in non-polar organic solvents like chloroform or dichloromethane, thanks to its aromatic structure.
  • Temperature Effect: The solubility can be affected by temperature; generally, solubility increases with rising temperature in most organic solvents.
  • pH Sensitivity: Being a pi-conjugated compound, its solubility might alter with changes in pH, affecting its ionization states.

Conclusion

In summary, while 3,4-dichloroisochromen-1-one has limited solubility in water and polar solvents, it demonstrates a stronger affinity towards non-polar solvents. Understanding the solubility behavior of this compound is crucial for applications in various chemical processes.

Interesting facts

Interesting Facts about 3,4-Dichloroisochromen-1-one

3,4-Dichloroisochromen-1-one is a fascinating chemical compound that belongs to the family of isoquinolines featuring multiple applications and unique properties. Here are some interesting points regarding this compound:

  • Versatile Building Block: This compound is often utilized in the synthesis of various pharmaceuticals and agrochemicals, acting as a versatile building block in organic chemistry.
  • Chirality in Chemistry: The presence of a fused isoquinoline structure enables intriguing chirality in certain derivatives, which can exhibit different biological activities.
  • Biological Activites: Research has shown that derivatives of 3,4-dichloroisochromen-1-one can possess anti-inflammatory and antioxidant properties, hinting at potential therapeutic uses.
  • Investigation of Fluorescence: The compound's electronic structure allows it to be explored for its fluorescent properties, which are of interest in fields such as materials science and biological imaging.
  • Environmental Considerations: Due to its chlorinated structure, understanding the degradation pathways of this compound in the environment is crucial for assessing its ecological impact.

As emphasized by many researchers, "The study of small organic molecules like 3,4-dichloroisochromen-1-one can lead to significant advancements in medicinal chemistry." This compound highlights the breadth of organic chemistry and its intersection with biological research, making it an intriguing target for future studies.

Synonyms
3,4-dichloroisocoumarin
51050-59-0
3,4-Dichloro-1H-isochromen-1-one
3,4-dichloroisochromen-1-one
3,4 dichloroisocoumarin
3,4-Dcl
3,4dichloroisocoumarin
3,4-DCI
1H-2-Benzopyran-1-one, 3,4-dichloro-
3,4-Dichloro-2-benzopyran-1-one
SD08W1HH6E
3,4-Dichloro-1H-2-benzopyran-1-one
MFCD00036960
NSC-727363
CHEMBL24983
CHEBI:109540
DTXSID70199056
NSC 727363
C9H4Cl2O2
3,4-dichloro-isocoumarin
Lopac-D-7910
UNII-SD08W1HH6E
cid_1609
Lopac0_000442
BSPBio_001549
KBioGR_000269
KBioSS_000269
MLS002153325
SCHEMBL106901
3,4-Dichloro-isochromen-1-one
KBio2_000269
KBio2_002837
KBio2_005405
KBio3_000537
KBio3_000538
DTXCID00121547
Bio2_000269
Bio2_000749
HMS1361N11
HMS1791N11
HMS1989N11
HMS3261I06
HMS3402N11
Tox21_500442
BDBM50199883
HSCI1_000089
NSC727363
PI-110
AKOS037649173
3,4-Dichloro-1H-isochromen-1-one #
CCG-204534
DB04459
LP00442
SDCCGSBI-0050427.P003
IDI1_034019
QTL1_000002
NCGC00015369-01
NCGC00015369-02
NCGC00015369-03
NCGC00015369-04
NCGC00015369-05
NCGC00015369-06
NCGC00015369-08
NCGC00093859-01
NCGC00093859-02
NCGC00093859-03
NCGC00261127-01
BS-16930
DA-69867
FD146840
PD002743
SMR001230738
HY-126034
CS-0090293
EU-0100442
NS00068269
D 7910
D81013
3,4-Dichloroisocoumarin serine protease inhibitor
3,4-Dichloroisocoumarin, serine protease inhibitor
SR-01000075831
SR-01000075831-1
BRD-K23704908-001-02-4
BRD-K23704908-001-03-2
Q27095241
637-085-4