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NBD Chloride

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Identification
Molecular formula
C6H3ClN3O3
CAS number
10199-89-0
IUPAC name
4-chloro-7-nitro-3-oxido-2,1,3-benzoxadiazol-3-ium
State
State

At room temperature, NBD chloride is in a solid state.

Melting point (Celsius)
-6.00
Melting point (Kelvin)
267.15
Boiling point (Celsius)
269.00
Boiling point (Kelvin)
542.00
General information
Molecular weight
186.55g/mol
Molar mass
186.5530g/mol
Density
1.6480g/cm3
Appearence

NBD chloride typically appears as a yellow crystalline solid.

Comment on solubility

Solubility of 4-chloro-7-nitro-3-oxido-2,1,3-benzoxadiazol-3-ium

The solubility of 4-chloro-7-nitro-3-oxido-2,1,3-benzoxadiazol-3-ium, often referred to as a specific heterocyclic compound, can be influenced by various factors. Here are some key points regarding its solubility:

  • Solvent Dependency: This compound is likely to be soluble in polar solvents such as water and organic solvents that can stabilize its ionic form.
  • Ionization: The presence of the ionizable -N+ group contributes to its solubility in aqueous solutions.
  • Hydrophobicity: The chlorine and nitro substituents may introduce some hydrophobic characteristics, possibly affecting overall solubility in non-polar solvents.

In summary, the solubility of 4-chloro-7-nitro-3-oxido-2,1,3-benzoxadiazol-3-ium is primarily characterized by a polar environment, with the potential for greater solubility in polar solvents due to its ionic nature and structural features.

Interesting facts

Interesting Facts about 4-Chloro-7-Nitro-3-Oxido-2,1,3-Benzoxadiazol-3-Ium

This compound is a fascinating member of the benzoxadiazole family, renowned for its diverse applications in various fields, particularly in chemical biology and material science. Here are some intriguing aspects to consider:

  • Versatile Applications: This compound is often utilized in the development of fluorescence-based sensors and probes, which are vital tools in biochemical assays.
  • Fluorescent Properties: The nitro and chloro groups attached to the benzoxadiazole ring enhance its photophysical properties, making it an excellent candidate for use in fluorescent imaging studies.
  • Biological Activity: It has shown potential in various biological contexts, including serving as a selective fluorescent label for the detection of specific biomolecules.
  • Structural Insights: The unique structure of this compound allows it to participate in hydrogen bonding, which can influence its behavior in biological systems and environmental interactions.

As a scientific community, we are constantly exploring the depths of such chemical compounds, discovering not only their functional properties but also their potential to unlock new pathways in research and innovation. From fundamental chemistry to practical applications, compounds like 4-chloro-7-nitro-3-oxido-2,1,3-benzoxadiazol-3-ium mark the synergy between molecular design and real-world utility.

Synonyms
18378-13-7
BENZOFURAZAN, 4-CHLORO-7-NITRO-, 3-OXIDE
4-Chloro-7-nitrobenzofurazan 3-oxide
UAK4GQ5BYC
NSC 228080
BRN 0533927
NSC-228080
DTXSID30171474
2,1,3-Benzoxadiazole, 4-chloro-7-nitro-, 3-oxide
DTXCID1093965
7-chloro-4-nitro-2,1,3-benzoxadiazole 1-oxide
NSC228080
UNII-UAK4GQ5BYC
SCHEMBL3509562
STK327650
AKOS000631941
2-chloro-5-nitro-9-oxido-8-oxa-7-aza-9-azoniabicyclo[4.3.0]nona-2,4,6,9-tetraene
DS-013120
ST50276327
7-chloro-4-nitrobenzo[c]1,2,5-oxadiazol-1-ol
AB00073860-01