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1,2,4-Trichloro-5-(3-iodoprop-2-ynoxy)benzene

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Identification
Molecular formula
C9H4Cl3IO
CAS number
156667-13-3
IUPAC name
1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene
State
State

At room temperature, this compound is a solid. Its structure and intermolecular interactions contribute to this solid state at ambient conditions.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.15
Boiling point (Celsius)
347.60
Boiling point (Kelvin)
620.75
General information
Molecular weight
365.44g/mol
Molar mass
365.4360g/mol
Density
1.7718g/cm3
Appearence

1,2,4-Trichloro-5-(3-iodoprop-2-ynoxy)benzene appears as a crystalline solid under standard conditions. The compound is typically white to off-white in color and can exhibit a distinct crystalline structure.

Comment on solubility

Solubility of 1,2,4-Trichloro-5-(3-iodoprop-2-ynoxy)benzene (C9H4Cl3IO)

The solubility of 1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene is influenced by several key factors, including its molecular structure and the presence of halogen substituents. This compound contains both chlorine and iodine atoms, which can affect its interaction with solvents. Here are some notable points regarding its solubility:

  • Polarity: The presence of chlorine and iodine may induce a certain degree of polarity, potentially affecting solubility in polar vs. non-polar solvents.
  • Solvents: It may exhibit higher solubility in non-polar or slightly polar organic solvents such as benzene, toluene, or dichloromethane due to its hydrophobic character.
  • Temperature Dependence: Solubility can increase with temperature; thus, it may be more soluble at elevated temperatures when tested in suitable organic solvents.
  • Concentration Effects: At higher concentrations, the solubility may reach a saturation point, leading to precipitation or crystallization in mixed solvent systems.

As with many halogenated compounds, it is crucial to consider environmental and safety implications, as their solubility characteristics may impact their behavior in biological systems and ecosystems.

Interesting facts

Interesting Facts about 1,2,4-Trichloro-5-(3-iodoprop-2-ynoxy)benzene

This intriguing compound, known as 1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene, showcases the fascinating blend of halogen chemistry and aromatic compounds. Here are some engaging points about this unique chemical:

  • Halogenated Nature: The presence of multiple chlorine atoms in its structure gives this compound significant chemical reactivity, making it a useful building block in medicinal chemistry and agricultural formulations.
  • Biological Activity: Compounds similar to this one often exhibit profound biological activities, increasing interest in their potential use in pest control and drug design. The iodine atom in the molecule may enhance its astringent properties.
  • Conjugated Systems: The presence of an alkyne group within the molecule enhances its conjugation, potentially leading to interesting optical properties, such as fluorescence or colorimetric changes when subjected to light.
  • Reactivity: Halogenated aromatic compounds are known for their varied and selective reactivity patterns, paving the way for complex chemical transformations in synthetic pathways.
  • Research and Applications: Ongoing research into halogenated compounds like this one often focuses on their role in creating novel materials, including polymers and molecular electronics, due to unique electronic properties.

In summary, 1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene is more than just a chemical entity; it encapsulates the intricate relationship between structure and function in organic chemistry—a potent hybrid of halogenated aromatic compounds with potential implications in various scientific fields.

Synonyms
haloprogin
777-11-7
Halotex
Mycanden
Haloprogine
Polik
Haloprogina
Mycilan
Haloproginum
M-1028 (Meiji)
1,2,4-trichloro-5-(3-iodoprop-2-ynoxy)benzene
Haloprogine [INN-French]
Haloproginum [INN-Latin]
Haloprogina [INN-Spanish]
M 1028
3-Iodo-2-propynyl 2,4,5-trichlorophenyl ether
2,4,5-Trichlorophenyl iodopropargyl ether
NSC-100071
Ether, 3-iodo-2-propynyl 2,4,5-trichlorophenyl
UNII-AIU7053OWL
EINECS 212-286-6
AIU7053OWL
NSC 100071
2,4,5-Trichlorophenyl gamma-iodopropargil ether
2,4,5-Trichlorophenyl-gamma-iodopropargyl ether
BRN 1976771
(3-Iod-2-propinyl)-(2,4,5-trichlorphenyl)ether
DTXSID9046865
Benzene, 1,2,4-trichloro-5-((3-iodo-2-propynyl)oxy)-
M-1028
NSC100071
CHEMBL1289
HALOPROGIN (200 MG)
DTXCID7026865
Haloprogin [USAN:USP:INN:JAN]
1,2,4-trichloro-5-[(3-iodoprop-2-yn-1-yl)oxy]benzene
NCGC00181134-01
Haloprogine (INN-French)
Haloproginum (INN-Latin)
Haloprogina (INN-Spanish)
HALOPROGIN (MART.)
HALOPROGIN [MART.]
1,2,4-Trichloro-5-((3-iodoprop-2-yn-1-yl)oxy)benzene
Benzene, 1,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]-
Haloprogin (USAN:USP:INN:JAN)
Halotex (TN)
component of Halotex
aloprogin
Haloprogen
Haloprogin (JAN/USAN/INN)
Prestwick_232
Halotex (Salt/Mix)
Spectrum_001852
HALOPROGIN [MI]
HALOPROGIN [INN]
HALOPROGIN [JAN]
HALOPROGIN [USAN]
HALOPROGIN [VANDF]
Ether,4,5-trichlorophenyl
SCHEMBL3649
HALOPROGIN [WHO-DD]
KBioSS_002369
2,4,5-Trichlorophenyl .gamma.-iodopropargyl ether
DivK1c_000762
1,2,4-trichloro-5-[(3-iodo-2-propynyl) oxy]benzene
CHEBI:5614
Benzene,1,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]
HALOPROGIN [ORANGE BOOK]
HMS502G04
KBio1_000762
KBio2_002365
KBio2_004933
KBio2_007501
WLN: I1UU2OR BG DG EG
D01AE11
NINDS_000762
HMS3713A06
BCP20218
Tox21_112741
BDBM50194601
AKOS030627167
CCG-220402
DB00793
2,5-Trichlorophenyl iodopropargyl ether
IDI1_000762
NCGC00181134-02
NCGC00181134-04
CAS-777-11-7
DA-53829
HY-16246
CS-0006262
NS00004428
3-Iodo-2-propynyl 2,5-trichlorophenyl ether
D00339
2,5-Trichlorophenyl .gamma.-iodopropargil ether
2,5-Trichlorophenyl .gamma.-iodopropargyl ether
EN300-8688382
1,2,4-trichloro-5-(3-iodoprop-2-ynyloxy)benzene
Q5643439
1,2,4-Trichloro-5-(3-iodo-prop-2-ynyloxy)-benzene
Benzene,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]-
BRD-K13238168-001-01-2
BRD-K13238168-001-02-0
212-286-6
Haloprogin; Benzene, 1,2,4-trichloro-5-[(3-iodo-2-propyn-1-yl)oxy]-; Benzene, 1,2,4-trichloro-5-[(3-iodo-2-propynyl)oxy]- (9CI); Ether, 3-iodo-2-propynyl 2,4,5-trichlorophenyl (7CI,8CI); 1,2,4-Trichloro-5-[(3-iodo-2-propyn-1-yl)oxy]benzene; 2,4,5-Trichlorophenyl ?-io