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Identification
Molecular formula
C20H28ClN2O4
CAS number
212430-94-3
IUPAC name
(4-nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, this compound is typically in a solid state, specifically a crystalline powder.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
341.81g/mol
Molar mass
341.8130g/mol
Density
1.1900g/cm3
Appearence

The compound appears as a white to off-white crystalline powder. The presence of the 4-nitrophenyl group can influence slight yellowish tinge

Comment on solubility

Solubility of (4-nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

The solubility of (4-nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride is influenced by several factors, including its ionic nature and the presence of the ammonium group. Here are some key points to consider:

  • Ionic Compounds: As an ammonium salt, this compound is likely to be soluble in water due to the ionic interactions with water molecules.
  • Hydrophilic Character: The presence of the 4-nitrophenyl group may contribute to a greater hydrophilic character, enhancing solubility in polar solvents.
  • Solvent Interaction: Its solubility can be affected by the nature of the solvent. While it exhibits good solubility in water, it may have variable solubility in organic solvents.

Ultimately, the solubility of this compound can be described as:

  1. High solubility in water due to its ionic dissolution.
  2. Variable solubility in organic solvents, often depending on the solvent's polarity.

Understanding these aspects of solubility helps in predicting the behavior of the compound in various chemical environments.

Interesting facts

Interesting Facts about (4-Nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium; Chloride

(4-Nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium; chloride is a fascinating compound with a range of applications in the world of chemistry. Here are some key points that highlight its significance:

  • Structure and Formation: The compound features a complex structure that includes both a phenyl group and a norbornane skeleton, combined with an ammonium moiety. This unique architecture often leads to interesting physical and chemical properties.
  • Pharmacological Interest: Compounds with similar structures have been explored for their biological activities. The nitrophenyl group can influence interactions with biological targets, making such analogs potential candidates in medicinal chemistry.
  • Reaction Chemistry: The presence of a nitro group typically enhances electrophilicity, allowing for various substitution reactions. This can make the compound useful in synthetic organic chemistry for the preparation of more complex molecules.
  • Potential Uses: The compound could excel in applications ranging from drug development to materials science, thanks to its multifaceted nature. Its interactions can be fine-tuned, which is crucial for developing new therapeutic agents.
  • Environmental Aspects: Understanding the stability and degradation pathways of such compounds is essential to assess their environmental impact, especially in pharmacology where the disposal of pharmaceuticals is a growing concern.

In summary, (4-nitrophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium; chloride is more than just a chemical formulation. It represents a crossroads of molecular design, biological potential, and environmental considerations, making it a compound worthy of further exploration in the field of chemistry.

Synonyms
(+-)-endo-N-(p-Nitrobenzyl)-2-bornanamine hydrochloride
24629-62-7
2-BORNANAMINE, N-(p-NITROBENZYL)-, HYDROCHLORIDE, endo-(+-)-
RefChem:256684