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Dicycloheptyl-1,4-dihydroxyanthraquinone diimide

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Identification
Molecular formula
C34H22N2O6
CAS number
106-17-8
IUPAC name
N-(28-benzamido-6,13,19,26-tetraoxo-16-azaheptacyclo[15.12.0.02,15.05,14.07,12.018,27.020,25]nonacosa-1(29),2(15),3,5(14),7(12),8,10,17,20,22,24,27-dodecaen-8-yl)benzamide
State
State

The compound is in a solid state at room temperature, often appearing as fine crystals or a crystalline powder.

Melting point (Celsius)
254.00
Melting point (Kelvin)
527.15
Boiling point (Celsius)
560.00
Boiling point (Kelvin)
833.15
General information
Molecular weight
506.55g/mol
Molar mass
506.5470g/mol
Density
1.3675g/cm3
Appearence

The compound appears as a solid. It is typically characterized by being colored, often presenting as vivid yellow to orange crystals or powder, depending on the specific synthesis and purification methods.

Comment on solubility

Solubility of N-(28-benzamido-6,13,19,26-tetraoxo-16-azaheptacyclo[15.12.0.02,15.05,14.07,12.018,27.020,25]nonacosa-1(29),2(15),3,5(14),7(12),8,10,17,20,22,24,27-dodecaen-8-yl)benzamide

This compound exhibits interesting solubility characteristics due to its complex molecular structure. The presence of multiple functional groups can influence how the substance interacts with various solvents. Here are several key points about its solubility:

  • Polarity: The numerous polar groups in the compound contribute to its solubility in polar solvents, such as water and alcohols.
  • Solvent Compatibility: It tends to be less soluble in non-polar solvents; thus, it might require a tailored solvent system for effective dissolution.
  • Temperature Dependency: As with many compounds, increasing temperature can enhance solubility, potentially leading to higher dissolution rates.
  • Concentration Effects: At higher concentrations, precipitation may occur, indicating solubility limits.

As a rule of thumb, "like dissolves like" applies well here—polar solvents are more likely to facilitate solubilization. Researchers should consider using co-solvents if standard conditions do not yield satisfactory solubility. Overall, understanding the solubility of this compound is crucial for its application in various chemical processes.

Interesting facts

Interesting Facts about N-(28-benzamido-6,13,19,26-tetraoxo-16-azaheptacyclo[15.12.0.02,15.05,14.07,12.018,27.020,25]nonacosa-1(29),2(15),3,5(14),7(12),8,10,17,20,22,24,27-dodecaen-8-yl)benzamide

This intricate compound showcases the beauty of organic chemistry and the complex interactions involved within its structure. With a name that reflects its multifaceted nature, this molecule presents several fascinating aspects:

  • Diverse Functional Groups: The presence of amide linkages and multiple oxo (ketone) groups lends the compound unique chemical properties that can influence both reactivity and interactions with biological targets.
  • Cycloaliphatic Framework: The heptacyclic architecture implies a sophisticated spatial arrangement that can contribute to the compound’s stability and may have implications for steric effects and molecular recognition.
  • Potential Biological Applications: Due to its complex structure, this compound could be explored for pharmaceutical applications, particularly in the realm of drug design where specificity and affinity are crucial.
  • Intriguing Synthesis Pathways: The synthesis of such a multi-cyclic compound could involve various organic methodologies, showcasing significant skill in synthetic chemistry and possibly paving the way for innovative approaches in material science.
  • Applications in Materials Science: The unique structural characteristics may also lend this compound to applications in advanced materials, including coatings and polymers where tailored mechanical properties are desirable.

In the words of famous chemists, “A molecule is like a symphony; every atom plays an essential part in creating harmony.” With this compound, we find an intricate balance of complexity and functionality, making it a subject of continued research and admiration in the scientific community.

As we unravel the mysteries of such compounds, we also enhance our understanding of molecular design, opening new avenues for innovation in both chemistry and various applied sciences.

Synonyms
Vat Brown 3
131-92-0
C.I. VAT BROWN 3
Atic Vat Brown R
Caledon Brown R
Novatic Brown R
Tinon Brown GR
Tinon Brown GRF
Ahcovat Brown AR
Benzadone Brown R
Calcoloid Brown R
Ponsol Brown ARD
Amanthrene Brown R
Fenanthren Brown D
Mikethrene Brown R
Nyanthrene Brown R
Calcoloid Brown RK
Cibanone Brown FGR
Nihonthrene Brown R
Palanthrene Brown R
Pernithrene Brown R
Romantrene Brown FR
Leucosol Brown 3RN
Sandothrene Brown NR
Indanthren Brown FFR
Tyrian Brown I-FFR
Carbanthrene Brown AR
Vat Brown K
Ponsol Brown ARN
Cibanone Brown GR
Fenanthren Brown R
Indanthren Brown R
Tyrian Brown I-R
Indanthrene Brown R
Solanthrene Brown R
Calcoloid Brown RNB
Indanthrene Brown RN
Solanthrene Brown FR
Indanthren Brown RAP
Calcoloid Brown RNBC
Ahcovat Brown AR-BN
Indanthrene Brown RWP
Sandothrene Brown NRF
Carbanthrene Brown ARP
Caledon Brown R 300
Indanthrene Brown RARWP
Fenalac Brown VRA Supra Paste
CI Vat Brown 3
C.I. 69015
CCRIS 4892
EINECS 205-044-6
Vat-brown-3
BRN 0382039
9Z11GKO85B
Benzamide, N,N'-(10,15,16,17-tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho(2,3-a:2',3'-i)carbazole-4,9-diyl)bis-
NAVINON BROWN RSD
4-22-00-06652 (Beilstein Handbook Reference)
CI 69015
SOLANTHRENE BROWN F-R
N,N'-(10,15,16,17-Tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho(2,3-a:2',3'-i)carbazole-4,9-diyl)bis(benzamide)
DTXSID2026282
5H-Dinaphtho(2,3-a:2',3'-i)carbazole-5,10,15,17(16H)-tetrone, 4,9-dibenzamido-
N,N'-(10,15,16,17-Tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho[2,3-a:2',3'-I]carbazole-4,9-diyl)bis(benzamide)
ANTHRAGEN BROWN RA SUPRA PASTE 79-4016
Benzamide, N,N'-(10,15,16,17-tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho[2,3-a:2',3'-i]carbazole-4,9-diyl)bis-
Benzamide,N,N'-(10,15,16,17-tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho[2,3-a:2',3'-i]carbazole-4,9-diyl)bis-
N,N'-(5,10,15,17-Tetraoxo-10,15,16,17-tetrahydro-5H-dinaphtho[2,3-a:2',3'-i]carbazole-4,9-diyl)dibenzamide
N-(28-benzamido-6,13,19,26-tetraoxo-16-azaheptacyclo[15.12.0.02,15.05,14.07,12.018,27.020,25]nonacosa-1(29),2(15),3,5(14),7(12),8,10,17,20,22,24,27-dodecaen-8-yl)benzamide
UNII-9Z11GKO85B
Indanthrene Brown R (6CI)
5H-DINAPHTHO(2,3-A:2',3'-I)CARBAZOLE, BENZAMIDE DERIV.
5H-DINAPHTHO(2,3-A:2',3'-I)CARBAZOLE, BENZAMIDE DERIVATIVE
5H-DINAPHTHO[2,3-A:2',3'-I]CARBAZOLE, BENZAMIDE DERIV.
5H-DINAPHTHO[2,3-A:2',3'-I]CARBAZOLE, BENZAMIDE DERIVATIVE
5H-DINAPHTHO[2,3-A:2',3'-I]CARBAZOLE-5,10,15,17(16H)-TETRONE, 4,9-DIBENZAMIDO-
N,N'-(10,15,16,17-TETRAHYDRO-5,10,15,17-TETRAOXO-5H-DINAPHTHO-(2,3-A:2',3'-I)
N,N'-(10,15,16,17-TETRAHYDRO-5,10,15,17-TETRAOXO-5H-DINAPHTHO-[2,3-A:2',3'-I]
N,N'-(10,15,16,17-Tetrahydro-5,10,15,17-tetraoxo-5H-dinaphtho[2,3-a:2',3'-i]carbazole-4,9-diyl)bis[benzamide]
C.I Vat brown 3
INDANTHREN BROWN R-M
INDANTHRENE BROWN RAP
DTXCID206282
SCHEMBL3645960
HY-D0301
AKOS015913755
CARBAZOLE-4,9-DIYL)BISBENZAMIDE
C.I.Vat Brown 3 (C.I.69015)
CS-0010213
NS00020985
HELIO FAST BROWN R PRESSCAKE 79-4003
Q27273400
5H-Dinaphtho(2,3-a:2',3'-i)carbazole-5,10,15,17(16H)-tetrone, 4,9-dibenzamido-(7CI)
205-044-6