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2-(2-bromoethyl)isoindoline-1,3-dione

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Identification
Molecular formula
C10H8BrNO2
CAS number
3383-21-9
IUPAC name
2-(2-bromoethyl)isoindoline-1,3-dione
State
State

At room temperature, 2-(2-bromoethyl)isoindoline-1,3-dione is typically in a solid state. It remains stable when stored in a dry, cool environment and away from strong oxidizing agents.

Melting point (Celsius)
97.50
Melting point (Kelvin)
370.65
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
254.08g/mol
Molar mass
254.0780g/mol
Density
1.6098g/cm3
Appearence

2-(2-bromoethyl)isoindoline-1,3-dione typically appears as a crystalline solid with a pale, off-white coloration. It is often encountered in powdered form and is stable under standard conditions.

Comment on solubility

Solubility of 2-(2-bromoethyl)isoindoline-1,3-dione

The solubility of 2-(2-bromoethyl)isoindoline-1,3-dione can be influenced by several factors, including the presence of polar and nonpolar groups within its structure. Here are some key points regarding its solubility:

  • Polarity: The compound has both aromatic and aliphatic characteristics, which may lead to varying solubility in different solvents.
  • Solvent Interaction: It is likely to exhibit better solubility in polar solvents such as dimethyl sulfoxide (DMSO) or methanol, but may have limited solubility in nonpolar solvents like hexane or benzene.
  • Hydrogen Bonding: The functional groups present may engage in hydrogen bonding, further influencing its solubility in aqueous solutions.
  • Temperature Dependency: As with many organic compounds, solubility can increase with temperature, making it important to consider testing at various temperatures.

In conclusion, while precise numeric solubility values may vary, understanding the chemical interactions and structural elements of 2-(2-bromoethyl)isoindoline-1,3-dione is crucial for predicting its behavior in different solvent environments. Always test solubility empirically to confirm theoretical predictions!

Interesting facts

Facts About 2-(2-Bromoethyl)isoindoline-1,3-dione

The compound 2-(2-bromoethyl)isoindoline-1,3-dione is a fascinating member of the isoindoline family, known for its intriguing structure and potential applications. Here are some noteworthy points:

  • Structural Significance: This compound features a unique bicyclic structure that offers various sites for chemical reactivity, making it a valuable compound for synthetic organic chemistry.
  • Bromo Group Influence: The presence of the bromoethyl group enhances its electrophilic character, which can lead to further reactions with nucleophiles, expanding its utility in complex organic syntheses.
  • Biological Potential: Compounds of this type are often investigated for their biological activity. They may possess antitumor properties or other pharmacological activities, emphasizing the importance of isoindoline derivatives in medicinal chemistry.
  • Versatility in Synthesis: Due to its molecular structure, it serves as a versatile intermediate in the synthesis of other complex organic compounds, which can be useful in pharmaceuticals and agricultural chemistry.
  • Research Focus: Ongoing research into derivatives of isoindoline highlights the relevance of such compounds in developing new materials, dyes, and pharmaceuticals.

In summary, 2-(2-bromoethyl)isoindoline-1,3-dione exemplifies the intersection of organic synthesis, medicinal chemistry, and materials science. As chemists continue to explore this compound and its derivatives, the potential applications appear vast and promising.

Synonyms
N-(2-BROMOETHYL)PHTHALIMIDE
574-98-1
1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-
1-Bromo-2-phthalimidoethane
2-(Bromoethyl)phthalimide
beta-Phthalimidoethyl bromide
beta-Bromoethylphthalimide
Phthalimide, N-(2-bromoethyl)-
N-2-Bromoethylphthalimide
NSC 2688
EINECS 209-379-9
DTXSID0060357
DTXCID8042214
Phthalimide, N-(2-bromoethyl)-(8CI)
209-379-9
inchi=1/c10h8brno2/c11-5-6-12-9(13)7-3-1-2-4-8(7)10(12)14/h1-4h,5-6h
2-(2-bromoethyl)isoindoline-1,3-dione
2-(2-bromoethyl)isoindole-1,3-dione
2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione
MFCD00005902
2-(2-bromoethyl)-2,3-dihydro-1H-isoindole-1,3-dione
2-Phthalimidoethyl bromide
n(2-bromoethyl)phthalimide
.beta.-Bromoethylphthalimide
2-(2-Bromo-ethyl)-isoindole-1,3-dione
N-(Beta-bromoethyl)phthalimide
.beta.-Phthalimidoethyl bromide
NSC-2688
2-(2-bromoethyl)-isoindole-1,3-dione
2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione; 1-Bromo-2-phthalimidoethane; 2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethyl bromide; 2-(2-Bromoethyl)-2,3-dihydro-1H-isoindole-1,3-dione
N-(2-Bromoethyl)-phthalimide
N-Bromoethylphthalimide
phthalimidoethyl bromide
2-(2-bromoethyl)-1H-isoindole-1,3-dione
N-(bromoethyl)phthalimide
2-(2-bromoethyl)benzo[c]azoline-1,3-dione
N-(bromoethyl)-phthalimide
n(2-bromoethyl) phthalimide
N-(2-Bromoethyl)phthalimid
SCHEMBL53287
2-(2-Bromoethyl)phthalimide
N-beta-Bromoethyl-phthalimide
N-(2-Bromoethyl)-phthalimid
N-(2- bromoethyl)phthalimide
N-(2-bromo-ethyl)phthalimide
N-(2-bromoethyl) phthalimide
A85E8KM8J6
CHEMBL595355
N-(2-bromo ethyl)-phthalimide
N-(2-bromo-ethyl)-phthalimide
N-[2-(bromo)ethyl]phthalimide
NSC2688
N-(.beta.-Bromoethyl)phthalimide
ALBB-017759
N-(2-Bromoethyl)phthalimide, 95%
AC-165
STK291118
AKOS000119699
1H-Isoindole-1, 2-(2-bromoethyl)-
CS-W008910
2-(2-Bromo-ethyl)isoindole-1,3-dione
2-(2-bromoethyl) isoindoline-1,3-dione
AS-11033
BP-13404
SY002569
DB-002815
B0597
NS00033738
EN300-17894
AE-641/00791032
2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione #
Z57069240
F3380-0002
2-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-ethyl bromide