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AEBSF

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Identification
Molecular formula
C8H10FNO2S
CAS number
30827-99-7
IUPAC name
4-(2-aminoethyl)benzenesulfonyl fluoride
State
State
At room temperature, AEBSF is present in a solid state, specifically as a crystalline powder.
Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
201.24g/mol
Molar mass
201.2350g/mol
Density
1.3650g/cm3
Appearence
AEBSF typically appears as a white to off-white crystalline powder.
Comment on solubility

Solubility of 4-(2-aminoethyl)benzenesulfonyl fluoride (C8H10FNO2S)

4-(2-aminoethyl)benzenesulfonyl fluoride, a compound known for its unique structure, displays interesting solubility characteristics that influence its application and behavior in various solvents.

Solubility in Different Solvents

This compound is generally soluble in a variety of polar solvents, thanks to the presence of its polar functional groups. Notably:

  • Water: Moderately soluble due to the amino and sulfonyl functional groups which can interact favorably with water molecules.
  • Alcohols: Highly soluble in alcohols like ethanol and methanol, which offer both hydrogen bonding opportunities and enhanced solvation.
  • Apolar Solvents: Displays low solubility in apolar solvents such as hexane, owing to its polar group hindering dissolution.

Key Factors Influencing Solubility

The solubility profile of 4-(2-aminoethyl)benzenesulfonyl fluoride can be attributed to:

  • Polarity: The presence of nitrogen and fluorine atoms contributes to an overall dipole moment, enhancing interactions with polar solvents.
  • Hydrogen Bonding: Capable of forming hydrogen bonds due to the amino group, which can interact effectively in solvent matrices.
  • Size and Structure: The bulky aromatic ring can hinder solubility in non-polar environments but aids in compatibility with more polar solvents.

In conclusion, the solubility behavior of 4-(2-aminoethyl)benzenesulfonyl fluoride makes it a versatile compound, adaptable to various chemical environments, and significant in chemical synthesis and applications.

Interesting facts

Interesting Facts about 4-(2-aminoethyl)benzenesulfonyl fluoride

4-(2-aminoethyl)benzenesulfonyl fluoride is a fascinating compound with notable applications and characteristics. Here are some engaging insights:

  • Structure and Functionality: This compound contains a sulfonyl fluoride group, which is known for its reactivity in chemical synthesis. Sulfonyl fluorides are considered excellent electrophiles, making this compound particularly useful in various chemical reactions.
  • Biological Relevance: Compounds with aminoethyl groups often exhibit biological activity. The presence of both the amino group and the sulfonyl fluoride may position this molecule as a potential candidate for drug development, especially in targeting specific biological systems.
  • Synthetic Versatility: The unique structure allows for versatile modifications. This compound can serve as a building block in the synthesis of more complex molecules, particularly in the pharmaceutical industry.
  • Reactivity: The sulfonyl fluoride moiety is particularly reactive toward nucleophiles. This property can lead to useful applications in creating new molecular frameworks and functionalized compounds.
  • Applications: While specific applications can depend on the context, it may find use in areas such as materials science, medicinal chemistry, and agrochemicals. The functional groups present allow chemists to explore sophisticated reaction mechanisms.

As stated by chemists, “Understanding the reactivity and potential of compounds like 4-(2-aminoethyl)benzenesulfonyl fluoride opens the door to innovative research and applications.”

In summary, 4-(2-aminoethyl)benzenesulfonyl fluoride is not just a compound of theoretical interest; it embodies the bridge between chemical structure and practical application, encouraging ongoing exploration and appreciation in the field of chemistry.

Synonyms
4-(2-Aminoethyl)benzenesulfonyl fluoride
34284-75-8
AEBSF
4-(2-Aminoethyl)benzenesulfonylfluoride
4-(2-aminoethyl)benzene-1-sulfonyl fluoride
4-beta-Aminoethylbenzolsulfofluoride
Benzenesulfonyl fluoride, 4-(2-aminoethyl)-
F5D36L5354
DTXSID40187844
AES
CHEMBL1256178
AEBSF cpd
SR-01000075690
ABSF
4-2(aminoethyl)-benzensulfonyl fluoride
Lopac-A-8456
Lopac0_000132
SCHEMBL77781
CHEMBL1096339
UNII-F5D36L5354
DTXCID00110335
BDBM50398077
CCG-204227
DB07347
SDCCGSBI-0050120.P002
NCGC00015097-01
NCGC00015097-02
NCGC00015097-03
NCGC00015097-12
NCGC00162071-01
PD005322
NS00015316
[4-(2-Aminoethyl)-benzenesulphonyl fluoride]
G22633
EN300-1581783
Q290992
BENZENESULFONYL FLUORIDE, P-(2-AMINOETHYL)-
SR-01000075690-6