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Cryptophane-A

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Identification
Molecular formula
C42H54O6N6
CAS number
86439-84-1
IUPAC name
3,6,9,15,18,21,27,30,33-nonaisopropyl-12,24,36-trimethyl-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone
State
State
Cryptophane-A is a solid at room temperature, typically found as a white crystalline material.
Melting point (Celsius)
233.00
Melting point (Kelvin)
506.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
930.15g/mol
Molar mass
930.1540g/mol
Density
1.0500g/cm3
Appearence

Cryptophane-A appears as a white crystalline solid that is typically formed as powder or small crystals. It is often used in research settings and has a well-defined crystalline structure.

Comment on solubility

Solubility of 3,6,9,15,18,21,27,30,33-nonaisopropyl-12,24,36-trimethyl-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone (C42H54O6N6)

The solubility of a compound such as 3,6,9,15,18,21,27,30,33-nonaisopropyl-12,24,36-trimethyl-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone is particularly complex. Here are some factors influencing its solubility:

  • Molecular Structure: The extensive branching and bulky isopropyl groups can hinder the interaction with solvent molecules, affecting solubility.
  • Polarity: The presence of oxygen and nitrogen can introduce polarity, but the overall large hydrophobic carbon backbone may lead to low solubility in polar solvents.
  • Solvent Compatibility: This compound is more likely to be soluble in non-polar organic solvents due to its large hydrocarbon content. Compatibility with solvents such as hexane or chloroform may be favorable.
  • Temperature Effects: Increased temperature often increases solubility for many organic compounds, which may aid in dissolving such intricate structures.

In conclusion, this compound's solubility is expected to be low in polar solvents and potentially higher in non-polar solvents. "The nature of solubility is dictated by the delicate balance of intermolecular forces and molecular structure."

Interesting facts

Interesting Facts about 3,6,9,15,18,21,27,30,33-nonaisopropyl-12,24,36-trimethyl-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone

This complex molecular structure, with its extensive array of functional groups and cyclic components, presents a fascinating topic in the field of chemistry. Here are some intriguing points:

  • Structural Complexity: This compound contains numerous isopropyl and methyl groups, leading to a branched structure that can affect its chemical reactivity and stability.
  • Use in Materials Science: Given its wide range of functional groups, this compound might have applications in polymer science, potentially serving as a precursor for novel materials with unique properties.
  • Bioactivity: Compounds with multiple nitrogen atoms, as seen in this structure, are often investigated for their biological activity. There's the potential for this compound to exhibit interesting pharmaceutical properties.
  • Synthetic Challenges: The synthesis of such a large and complex molecule demands advanced skills in organic synthesis, highlighting the challenges and rewards of modern chemistry.
  • Research Potential: As a member of the dodecone family, understanding this compound could open up new avenues in the study of fragrance chemistry, possibly leading to novel perfumes.

As we examine the various aspects of this compound, one can't help but be inspired by how intricate chemical structures can lead to a myriad of potential applications in science, highlighting the endless creativity inherent in chemical research. As the chemist Linus Pauling once said, "The best way to have a good idea is to have many ideas." This compound exemplifies just that, serving as a gateway to numerous possibilities in the world of chemistry.

Synonyms
valinomycin
Valinomicin
2001-95-8
GNF-Pf-5297
NSC 122023
(+)-VALINOMYCIN
SCHEMBL41016
BSPBio_001226
KBioGR_000566
KBioGR_002478
KBioSS_000566
KBioSS_002485
CHEMBL602575
CHEBI:95123
KBio2_000566
KBio2_002478
KBio2_003134
KBio2_005046
KBio2_005702
KBio2_007614
KBio3_001011
KBio3_001012
KBio3_002956
cMAP_000062
Bio1_000384
Bio1_000873
Bio1_001362
Bio2_000453
Bio2_000933
HMS1362N07
HMS1792N07
HMS1990N07
HMS3403N07
Cyclo(D-.alpha.-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-.alpha.-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl-D-.alpha.-hydroxyisovaleryl-D-valyl-L-lactoyl-L-valyl)
Cyclo(L-Val-D-HyIva-D-Val-L-Lac-)3: HyIva = alpha-Hydroxyisovaleric acid, Lac = Lactic acid
BDBM50420225
AKOS024319642
IDI1_002208
NCGC00095987-01
NCGC00095987-02
NCGC00095987-03
6,18,30-trimethyl-3,9,12,15,21,24,27,33,36-nona(propan-2-yl)-1,7,13,19,25,31-hexaoxa-4,10,16,22,28,34-hexazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone
LS-15509
Q27166904
1,13,19,25,31-Hexaoxa-4,10,16,22,28,34-hexaazacyclohexatriacontane-2,5,8,11,14,17,20,23,26,29,32,35-dodecone, 12,24,36-trimethyl-3,6,9,15,18,21,27,30,33-nonakis(1-methylethyl)-
WLN: T-36-MV DOV GMV JOV MMV POV SMV VOV B&MV E&OV H&MV K&OVTJ CY1&1 FY1&1I1 LY1&1 OY1&1 RY1&1 U1 A&Y1&1 D&Y1&1 G&Y1&1 J&1 M&Y1&1