Skip to main content

Indeno[2,1-c]chromene pentol

ADVERTISEMENT
Identification
Molecular formula
C17H16O5
CAS number
72623-21-9
IUPAC name
7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol
State
State

At room temperature, this compound is typically found in a solid state. Its structure is stable under normal conditions, but it should be handled with care to prevent decomposition or reaction due to environmental factors such as humidity or light exposure.

Melting point (Celsius)
243.00
Melting point (Kelvin)
516.15
Boiling point (Celsius)
486.00
Boiling point (Kelvin)
759.15
General information
Molecular weight
304.28g/mol
Molar mass
304.2770g/mol
Density
1.3425g/cm3
Appearence

The compound typically appears as a crystalline solid. It may present either as a colorless or pale yellow substance depending on purity. The appearance can vary slightly if crystallized from different solvents or if impurities are present.

Comment on solubility

Solubility of 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol

The solubility of 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol can significantly influence its behavior in various applications. Understanding its solubility characteristics is crucial for researchers and industry professionals.

Key Points about Solubility:

  • Solvent Dependency: The solubility of this compound is heavily affected by the type of solvent used. Polar solvents tend to enhance solubility due to the compound's functional hydroxyl groups.
  • Hydrogen Bonding: The presence of multiple hydroxyl (-OH) groups allows for extensive hydrogen bonding, which can increase solubility in water and polar organic solvents.
  • Temperature Influence: As with many compounds, solubility typically increases with temperature, making it important to consider heating during dissolution processes.
  • Chemical Stability: The stability of the compound in solution can also affect solubility; care should be taken as some solvents may lead to degradation.

In summary, the solubility of 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol is influenced by various factors including solvent choice, temperature, and chemical interactions. Understanding these factors is essential for effective use in practical applications.

Interesting facts

Interesting Facts about 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol

The compound 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol is a fascinating molecule that reflects the beauty of organic chemistry and its applications. Here are some interesting aspects of this compound:

  • Structure & Functionality: This compound is characterized by its unique bicyclic structure that incorporates both indene and chromene motifs. This integration allows it to exhibit properties that are beneficial in various chemical reactions.
  • Biological Significance: Research suggests that compounds like this one may possess biological activities, including potential antioxidant and anti-inflammatory effects. Understanding such properties can open pathways for therapeutic applications.
  • Synthesis Pathways: The synthesis of this compound can involve innovative organic reactions, which may serve as a study topic for chemistry students looking to explore techniques like cross-coupling and cyclization reactions.
  • Potential Applications: The intriguing structure of 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol suggests its utility in medicinal chemistry, particularly in drug design and development.

The exploration of this compound can be an illuminating experience, highlighting how through understanding molecular design, scientists can unlock new functionalities and applications. As one notable chemist puts it, "The possibilities are as endless as the imagination itself."

Overall, compounds like 7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol are more than just structures; they are gateways to new science!

Synonyms
7,11b-dihydrobenz[b]indeno[1,2-d]pyran-3,4,6a,9,10(6H)-pentol
Benz(b)indeno(1,2-d)pyran-3,4,6a,9,10(6H)-pentol, 7,11b-dihydro-, (6aS,11bR)-
Benz[b]indeno[1,2-d]pyran-3,4,6a,9,10(6H)-pentol, 7,11b-dihydro-, (6aS,11bR)-
7,11b-dihydrobenz(b)indeno(1,2-d)pyran-3,4,6a,9,10(6H)-pentol
NSC8662
7,11b-Dihydroindeno[2,1-c]chromene-3,4,6a,9,10(6H)-pentol
17647-60-8
Hematoxyline
Hematoxylin, Trihydrate
7,11b-dihydro-6H-indeno[2,1-c]chromene-3,4,6a,9,10-pentol
MLS000876743
CHEBI:51686
SMR000440556
7,11b-Dihydroindeno(2,1-c)chromene-3,4,6a,9,10(6H)-pentol
6,6a,7,11b-tetrahydroindeno[2,1-c]chromene-3,4,6a,9,10-pentaol
Benz[b]indeno[1,2-d]pyran-3,4,6a,9,10(6H)-pentol, 7,11b-dihydro-
1412-19-7
1621-46-1
cid_10603
Benz(b)indeno(1,2-d)pyran-3,4,6a,9,10(6H)-pentol, 7,11b-dihydro-
rel-(6aS,11bR)-6,6a,7,11b-Tetrahydroindeno[2,1-c]chromene-3,4,6a,9,10-pentaol
CI 75290
NSC 8662
Hematoxylin trihydrate
Spectrum_000797
SpecPlus_000254
Spectrum2_000599
Spectrum3_000689
Spectrum4_001433
Spectrum5_000286
Oprea1_396303
Oprea1_483213
BSPBio_002417
KBioGR_001906
KBioSS_001277
SPECTRUM200010
MLS006011903
DivK1c_006350
HEMOTOXYLIN, TRIHYDRATE
SPBio_000478
MEGxp0_001929
SCHEMBL1784957
CHEMBL1479103
ACon0_001480
ACon1_000295
KBio1_001294
KBio2_001277
KBio2_003845
KBio2_006413
KBio3_001637
DTXSID00859439
WZUVPPKBWHMQCE-UHFFFAOYSA-N
BDBM114395
HMS2270H09
Hematoxylin Certified for Microscopy
NSC-8662
BBL023455
CCG-38519
NSC167385
STL066314
AKOS000501606
AKOS016038565
NSC-167385
SDCCGMLS-0066451.P001
SMP1_000072
NCGC00095460-01
NCGC00095460-02
NCGC00095460-03
NCGC00095460-04
NCGC00095460-05
NCGC00095460-06
VS-07435
EU-0078154
NS00015351
AH-034/32856041
SR-01000758981
SR-01000758981-2
Q27122713
7,11b-Dihydrobenzo[b]indeno[1,2-d]pyran-3,4,6a,9,10(6H)-pentol
7,11b-Dihydroindeno[2,1-c]chromene-3,4,6a,9,10(6H)-pentol #
7,11b-dihydro-6H-indeno[2,1-c][1]benzopyran-3,4,6a,9,10-pentol
8-OXATETRACYCLO[8.7.0.0(2),?.0(1)(2),(1)?]HEPTADECA-2(7),3,5,12,14,16-HEXAENE-5,6,10,14,15-PENTOL