Interesting facts
Interesting Facts About 1,1-Dichloro-N-phenyl-methanimine
1,1-dichloro-N-phenyl-methanimine is a fascinating compound that embodies the intricate interplay of chemistry and application. Here are some noteworthy points to consider:
- Dual Functionality: This compound features both chloro and amine functional groups, which may contribute to its reactivity and potential use in various chemical syntheses.
- Research Relevance: Its structure makes it a subject of interest in organic synthesis, especially in the development of novel pharmaceutical agents. Compounds with similar structures have shown biological activity.
- Environmental Considerations: The presence of dichloro groups highlights the need to study its environmental impact and degradation pathways, as halogenated compounds can pose ecological risks.
- Mechanism Understanding: Studying the reactivity of 1,1-dichloro-N-phenyl-methanimine can provide insights into reaction mechanisms, opening avenues for the discovery of new synthetic routes.
- Place in Material Science: The compound may also have implications in materials science, particularly in the formulation of polymers and resins that require specific functional groups for enhanced properties.
In the words of one researcher, "Understanding the chemistry behind compounds like 1,1-dichloro-N-phenyl-methanimine is crucial for innovation in diverse fields, from pharmaceuticals to environmental science." This highlights its significance as a compound worthy of deeper investigation.
Synonyms
Phenylcarbylamine chloride
622-44-6
Phenyliminophosgene
Phenylcarbonimidic dichloride
N-Phenylimidophosgene
Phenylisocyanide dichloride
Carbonimidic dichloride, phenyl-
N-(Dichloromethylene)aniline
Phenyliminocarbonyl dichloride
Phenylisonitrile dichloride
Phenyl carbylamine chloride
1,1-dichloro-N-phenylmethanimine
Phenyl isocyanide, dichloride
Imidocarbonyl chloride, phenyl-
N-Phenylcarbimide dichloride
PHENYLIMIDOCARBONYL CHLORIDE
Aniline, N-dichloromethylene-
Carbonic dichloride, (phenylimino)-
Benzenamine, N-(dichloromethylene)-
N-Phenylcarbonimidic dichloride
N-Phenyliminocarbonyl dichloride
N-Phenylimino carbonyl dichloride
Chlorure de phenylcarbyl-amine
HSDB 1255
NSC 2051
EINECS 210-735-0
UN1672
BRN 2041123
Chlorure de phenylcarbyl-amine [French]
84XDL272K2
NSC-2051
DTXSID6074833
N-PHENYLIMIDOYL DICHLORIDE
3-12-00-00905 (Beilstein Handbook Reference)
PHENYLIMIDOCARBONYL CHLORIDE [HSDB]
NPhenylimidophosgene
NPhenylcarbimide dichloride
Aniline, Ndichloromethylene
N(Dichloromethylene)aniline
Chlorure de phenylcarbylamine
NPhenylcarbonimidic dichloride
Imidocarbonyl chloride, phenyl
NPhenyliminocarbonyl dichloride
Carbonimidic dichloride, phenyl
N-(PHENYLIMINO)PHOSGENE
NPhenylimino carbonyl dichloride
DTXCID0043266
Benzenamine, N(dichloromethylene)
Carbonic dichloride, (phenylimino)
DICHLORO(PHENYLIMINO)METHANE
(PHENYLIMINO)CARBONYL DICHLORIDE
Carbonimidic dichloride, phenyl-(9CI)
Phenyl isocyanide dichloride
UNII-84XDL272K2
Phenylcarbylaminchlorid
1-chloro-N-phenylmethanecarbonimidoyl chloride
Phenylisocyanide, dichloride
WLN: MU1R &GH
SCHEMBL8587959
NSC2051
carbonimidic dichloride, N-phenyl-
Phenyl isocyanide dichloride, 98%
AKOS028110534
FP178937
NS00034973
P0933
G83728
EN300-7077843
Phenylcarbylamine chloride [UN1672] [Poison]
Q27269563
Solubility of 1,1-Dichloro-N-phenyl-methanimine
The solubility of 1,1-dichloro-N-phenyl-methanimine can be quite intriguing, as it presents unique characteristics based on its chemical structure. To better understand its behavior in various solvents, consider the following points:
In summary, while the solubility of 1,1-dichloro-N-phenyl-methanimine is influenced by several factors, it is crucial to conduct specific tests in different solvents to achieve a comprehensive understanding of its solubility profile. Always keep in mind that “solubility is a balance of molecular interactions,” which can vary widely between different solvents and conditions.