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cyclohexylideneamino hexylcarbamate

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Identification
Molecular formula
C21H36N2O4
CAS number
123456-78-9
IUPAC name
(cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate
State
State

The compound is in a solid state at room temperature with crystalline properties, generally appearing as a powder.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
385.57g/mol
Molar mass
385.5730g/mol
Density
1.0230g/cm3
Appearence

This compound appears as a white to off-white crystalline powder. Its physical form is typically in solid state, and it has a characteristic odor.

Comment on solubility

Solubility of (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate

The compound (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate, with the chemical formula C21H36N2O4, exhibits particular solubility characteristics that are influenced by its molecular structure. Understanding its solubility is essential for applications in various chemical processes. Here are some key points to consider:

  • Polarity: The compound contains multiple functional groups that can affect its solubility in different solvents. The presence of the carbamate group suggests potential solubility in polar solvents like water, albeit limited.
  • Hydrophobic Regions: The cyclohexylidene groups introduce hydrophobic characteristics, which may lead to reduced solubility in highly polar solvents but may increase solubility in organic solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds, especially through the amino and carbamate functionalities, can enhance its solubility in polar protic solvents.
  • Temperature Effects: Like many organic compounds, the solubility may increase with temperature, making it beneficial to consider operational conditions during its application.

In summary, while (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate exhibits some degree of solubility in polar solvents, its overall solubility profile is considerably influenced by both its polarity and the introduction of hydrophobic cyclohexylidene groups. Further experimental exploration could provide valuable insight into its behavior in various solvents, allowing for optimized usage in laboratories and industrial processes.

Interesting facts

Interesting Facts about (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate

(cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate is a fascinating compound that showcases the intricate and unique world of organic chemistry. This compound is characterized by its multifunctional structure, comprised of various chemical moieties that can lead to diverse applications in numerous fields.

Chemical Structure and Characteristics

  • Complexity: The presence of both carbamate and amino groups within this compound illustrates the potential for hydrogen bonding, which can significantly influence its reactivity and interactions with biological systems.
  • Versatility: The cyclic structure and the use of cyclohexylidene groups suggest that this compound may demonstrate interesting conformational behaviors, which are essential for understanding and predicting its chemical behavior.
  • Potential Applications: Compounds like this one are often explored in medicinal chemistry for their therapeutic properties. The design of multifaceted molecules can lead to enhanced bioactivity and selectivity in drug development.

Research Insights

Research into compounds of this nature often delves into:

  • The exploration of new synthetic pathways.
  • Investigating their biological activity as potential drug candidates.
  • Understanding their environmental stability and degradation products.

As a result, studies involving (cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate can provide valuable insights into how such compounds interact at a molecular level, paving the way for innovative applications in pharmaceuticals and beyond.

Conclusion

In summary, the compound exemplifies the beauty of chemical complexity, and studying it can yield important knowledge about the design and function of new materials and therapies. The multidisciplinary nature of its applications makes it an exciting area of research for both chemists and pharmacologists alike.

Synonyms
Rhc 80267
83654-05-1
RHC-80267
RHC80267
1,6-Bis(cyclohexyloximinocarbonyl)hexane
U 57908
1,6-BIS(CYCLOHEXYLOXIMINOCARBONYLAMINO)HEXANE
U-57908
1,6-Di(O-(carbamoyl)cyclohexanone oxime)hexane
Cyclohexanone O-((6-((((cyclohexylideneamino)oxy)carbonyl)amino)hexyl)carbamoyl) oxime
9VB68H5WIT
CHEMBL158897
cyclohexylideneamino N-[6-({[(cyclohexylideneamino)oxy]carbonyl}amino)hexyl]carbamate
cyclohexanone O-6-((cyclohexylideneaminooxy)carbonylamino)hexylcarbamoyl oxime
Rg 80267
CBiol_002009
Rg80267
(cyclohexylideneamino) N-[6-[(cyclohexylideneamino)oxycarbonylamino]hexyl]carbamate
Cyclohexanone, O,O'-(1,6-hexanediylbis(iminocarbonyl))dioxime
UNII-9VB68H5WIT
BSPBio_001074
KBioGR_000414
KBioSS_000414
GTPL5255
SCHEMBL23015112
BCBcMAP01_000181
CHEBI:92984
KBio2_000414
KBio2_002982
KBio2_005550
KBio3_000787
KBio3_000788
DTXSID90232494
Bio1_000295
Bio1_000784
Bio1_001273
Bio2_000377
Bio2_000857
HMS1362F15
HMS1792F15
HMS1990F15
HMS3268I22
HMS3403F15
HMS3412J18
HMS3676J18
EX-A3809
BDBM50240877
MFCD00210844
AKOS024456809
RHC 80267?
IDI1_002132
NCGC00159531-01
NCGC00159531-02
NCGC00159531-03
NCGC00159531-04
AC-36871
BS-17712
DA-67189
HY-107416
CS-0028444
S0766
RHC 80267, >=98% (HPLC), solid
RHC-80267; U-57908
D81503
Q7320283
BRD-K56047318-001-02-2
BRD-K56047318-001-03-0
BRD-K56047318-001-06-3
RHC-80267 - CAS 83654-05-1
(Hexane-1,6-diyldiimino)bis{[(cyclohexylideneamino)oxy]methanone}
O,O'-((Hexane-1,6-diylbis(azanediyl))bis(carbonyl))dicyclohexanone oxime
CYCLOHEXANONE, 1,1'-(O,O'-(1,6-HEXANEDIYLBIS(IMINOCARBONYL))DIOXIME)
CyclohexanoneO-((6-((((cyclohexylideneamino)oxy)carbonyl)amino)hexyl)carbamoyl)oxime
N-[6-[[(cyclohexylideneamino)oxy-oxomethyl]amino]hexyl]carbamic acid (cyclohexylideneamino) ester