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5-(aminooxymethyl)-2-bromophenol

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Identification
Molecular formula
C7H8BrNO2
CAS number
16275-57-1
IUPAC name
5-(aminooxymethyl)-2-bromo-phenol
State
State

This compound is typically found in a solid state at room temperature.

Melting point (Celsius)
193.00
Melting point (Kelvin)
466.15
Boiling point (Celsius)
342.00
Boiling point (Kelvin)
615.15
General information
Molecular weight
231.05g/mol
Molar mass
232.0410g/mol
Density
1.6730g/cm3
Appearence

5-(Aminooxymethyl)-2-bromophenol is typically a solid substance. It may appear as a crystalline powder or a similar solid form.

Comment on solubility

Solubility of 5-(Aminooxymethyl)-2-bromo-phenol

The solubility of 5-(aminooxymethyl)-2-bromo-phenol can be influenced by various factors, including its molecular structure and the nature of the solvent. This compound, characterized by the presence of both amino and bromo functional groups, exhibits interesting solubility behavior.

Generally, the solubility can be assessed as follows:

  • In Water: The presence of the amino group suggests that 5-(aminooxymethyl)-2-bromo-phenol may have some degree of solubility in water due to hydrogen bonding capabilities.
  • In Organic Solvents: This compound may be more soluble in organic solvents, particularly those that are polar, such as methanol or ethanol, due to the overall hydrophobic structure imparted by the phenol ring and the bromo substituent.
  • pH Dependence: The solubility may also be pH-dependent; under acidic conditions, the amino group can become protonated, which might enhance solubility in water.

As a general insight, the solubility of many organic compounds, including 5-(aminooxymethyl)-2-bromo-phenol, can often be summarized by the phrase: “like dissolves like.” Thus, both the chemical structure and the choice of solvent are critical in determining how readily this compound will dissolve in a given environment.

Interesting facts

Interesting Facts about 5-(Aminooxymethyl)-2-bromo-phenol

5-(Aminooxymethyl)-2-bromo-phenol, often referred to in scientific literature as a phenolic compound, boasts an intriguing profile that bridges the fields of organic chemistry and medicinal applications. This compound can be appreciated for several noteworthy aspects:

  • Biological Activity: Compounds like 5-(aminooxymethyl)-2-bromo-phenol are extensively studied for their potential therapeutic properties. They often exhibit antibacterial and antifungal characteristics, making them of great interest in pharmaceutical research.
  • Synthetic Utility: The presence of the bromo substituent allows for versatile synthetic pathways, enabling chemists to easily modify the compound for various applications. This manipulation often leads to compounds that may have improved efficacy or enhanced biological activity.
  • Research Interest: The incorporation of the aminooxymethyl group provides interesting potential for drug interaction studies, as it can significantly impact the bioavailability and solubility of the compound in biological systems.
  • Analytical Importance: Due to its unique structure, 5-(aminooxymethyl)-2-bromo-phenol can serve as a useful standard in chromatographic techniques and mass spectrometry. It helps in developing methods for quantitative analysis of similar compounds.

This compound represents just one small part of a vast family of phenolic compounds, each with its unique properties and reactivity. As research continues, we can expect discoveries that may unlock further applications not yet imagined.

If you’re intrigued by the potential of organic compounds in medicinal chemistry, keeping an eye on 5-(aminooxymethyl)-2-bromo-phenol may lead to exciting insights and innovations!

Synonyms
Brocresine
555-65-7
Brocresin
Brocresina
3-(Aminooxymethyl)-6-bromphenol
NSD-1055
Brocresina [INN-Spanish]
Brocresinum
CL 54998
Brocresinum [INN-Latin]
5-[(Aminooxy)methyl]-2-bromophenol
Brocresine [USAN:INN:BAN]
Phenol, 5-((aminooxy)methyl)-2-bromo-
alpha-(Aminooxy)-6-bromo-m-cresol
5-((Aminooxy)methyl)-2-bromophenol
BRN 1945736
O-)4-Brom-3-hydroxybenzyl)hydroxylamin
4-Bromo-3-hydroxybenzyloxyamine
11F6O06WN0
CL 108,756
BROCRESINE [INN]
BROCRESINE [USAN]
.alpha.-(Aminooxy)-6-bromo-m-cresol
BROCRESINE [MART.]
CL-54998
CL-108756
m-CRESOL, alpha-(AMINOOXY)-6-BROMO-
DTXSID40204080
m-Cresol, .alpha.-(aminooxy)-6-bromo-
Brocresinum (INN-Latin)
Brocresina (INN-Spanish)
BROCRESINE (MART.)
DTXCID40126571
qnwosjagfsudfe-uhfffaoysa-n
NSD 1055
5-(aminooxymethyl)-2-bromophenol
NSD1055
UNII-11F6O06WN0
Brocresine (USAN/INN)
SCHEMBL635454
5-aminooxymethyl-2-bromo-phenol
CHEMBL2106020
GLXC-06485
AKOS037643546
AS-16839
HY-122968
NS00113991
D03158
EN300-211634
Q27251320