Skip to main content

Camphoric anhydride

ADVERTISEMENT
Identification
Molecular formula
C10H12O4
CAS number
124-11-8
IUPAC name
(1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione
State
State

Camphoric anhydride is a crystalline solid at room temperature with a stable, solid consistency. It is not volatile and typically does not evaporate at room temperature. When it sublimes, it turns directly from the solid into a vapor without becoming liquid, under suitable conditions.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.00
Boiling point (Celsius)
244.00
Boiling point (Kelvin)
517.00
General information
Molecular weight
168.17g/mol
Molar mass
168.1690g/mol
Density
1.1700g/cm3
Appearence

Camphoric anhydride is a white crystalline solid. It is typically colorless and appears as clear crystalline sheets, which are sparkling and twinkle under light. It is solid at room temperature and quite stable if kept dry.

Comment on solubility

Solubility of (1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione

The compound (1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione, with the chemical formula C10H12O4, exhibits noteworthy solubility characteristics that are influenced by its chemical structure.

Key factors affecting its solubility include:

  • Molecular Polarity: The presence of hydroxyl (–OH) groups increases the polarity, which may enhance solubility in polar solvents like water.
  • Hydrophobic Regions: The hydrocarbon portions may limit solubility in highly polar solvents.
  • Steric Hindrance: The three-dimensional arrangement of atoms may impede interactions with solvent molecules.

Typically, compounds of this nature see:

  • Higher solubility in organic solvents, such as ethanol and acetone.
  • Lower solubility in water, unless modified through chemical means.

In summary, while this compound may show some degree of solubility in both polar and non-polar solvents, understanding the balance between its hydrophilic and hydrophobic characteristics is crucial for predicting its behavior in various environments. As noted in the field, “the solubility is not just a property; it’s a reflection of the molecular intricacies that bind the ingredients of life.”

Interesting facts

Interesting Facts about (1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione

(1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione is a fascinating compound that holds significant interest in the field of organic chemistry due to its unique structure and potential applications. Here are some noteworthy aspects:

  • Synthetic Versatility: This compound shows promise for various synthetic routes, making it a valuable intermediate in organic synthesis. Its intricate structure provides opportunities to create more complex molecules.
  • Biological Activity: Compounds with dioxatricyclo structures often exhibit interesting biological activities. This particular compound may possess unique antimicrobial or antioxidant properties, paving the way for potential medicinal uses.
  • Chirality: The specific stereochemistry (1R, 2S, 6R, 7S) makes this compound a subject of interest in enantioselective synthesis, which is crucial in pharmaceuticals where single enantiomers are often more effective than their mixtures.
  • Research & Development: Ongoing research examines how modifications to this compound can enhance its properties or create derivatives with improved efficacy, particularly in drug design.

As expressed by chemist Robert H. Grubbs, "The beauty of chemistry lies in the ability to construct complex architectures from simple building blocks." This compound exemplifies that beauty through its intricate and versatile structure.

In summary, (1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione is more than just a chemical formula. It represents a world of possibilities in synthesis, medicinal applications, and biological research.

Synonyms
cantharidin
56-25-7
Cantharone
CANTHARIDINE
Kantaridin
Kantharidin
Cantharides camphor
Cantaridina
Cantharidinum
Kantharidin [German]
Caswell No. 157
(3ar,4s,7r,7as)-3a,7a-dimethylhexahydro-4,7-epoxy-2-benzofuran-1,3-dione
CAN [Alkaloid]
1,2-Dimethyl-3,6-epoxyperhydrophthalic anhydride
Cantharidin [USAN]
CCRIS 635
HSDB 2181
exo-1,2-cis-Dimethyl-3,6-epoxyhexahydrophthalic anhydride
AI3-04021
UNII-IGL471WQ8P
EINECS 200-263-3
NSC 61805
NSC-61805
EPA Pesticide Chemical Code 013101
BRN 0085302
YCANTH
CHEBI:64213
NSC61805
CANTHARIDIN [MI]
4,7-Epoxyisobenzofuran-1,3-dione, hexahydro-3a,7a-dimethyl-, (3aR,4S,7R,7aS)-rel-
CANTHARIDIN [INN]
MFCD00134968
CANTHARIDIN [IARC]
CANTHARIDIN [VANDF]
CANTHARIDINE [HSDB]
CANTHARIDIN [MART.]
CANTHARIDINUM [HPUS]
IGL471WQ8P
CANTHARIDIN [WHO-DD]
CHEMBL48449
2,3-Dimethyl-7-oxabicyclo(2.2.1)heptane-2,3-dicarboxylic anhydride
5-19-05-00051 (Beilstein Handbook Reference)
CAN (Alkaloid)
Hexahydro-3a,7a-dimethyl-4,7-epoxyisobenzofuran-1,3-dione
Hexahydro-3aalpha,7aalpha-dimethyl-4beta,7beta-epoxyisobenzofuran-1,3-dione
4,7-Epoxyisobenzofuran-1,3-dione, hexahydro-3a,7a-dimethyl-, (3a-alpha,4-beta,7-beta,7a-alpha)
Cantharidin (USAN)
CANTHARIDIN (IARC)
CANTHARIDIN (MART.)
Ycanth (0.7% solution, single-use topical applicator)
HEXAHYDRO-3A.ALPHA.,7A.ALPHA.-DIMETHYL-4.BETA.,7.BETA.-EPOXYISOBENZOFURAN-1,3-DIONE
7-Oxabicyclo(2.2.1)heptane-2,3-dicarboxylic anhydride, 2,3-dimethyl-
DTXCID5021752
(1R,5S,6R,9S)-REL-1,5-DIMETHYL-3,10-DIOXATRICYCLO(3.2.1.01,5)DECANE-2,4-DIONE
(1R,5S,6R,9S)-rel-1,5-Dimethyl-3,10-dioxatricyclo[3.2.1.01,5]decane-2,4-dione
(1S,2R,6S,7R)-2,6-dimethyl-4,10-dioxatricyclo(5.2.1.02,6)decane-3,5-dione
(1S,2R,6S,7R)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione
CAS-56-25-7
NCGC00016247-01
Ycanth (TN)
Prestwick3_000885
Cantharidin (JAN/USAN)
(1R,2S,3R,6S)-1,2-Dimethyl-3,6-epoxycyclohexane-1,2-dicarboxylic anhydride
2,3-dicarboxylic anhydride
7a-Dimethylhexahydro-3a,4,7-epoxyisobenzofuran
CANTHARIDIN 0.7%
NCIMech_000301
BSPBio_000670
SCHEMBL152262
BPBio1_000738
cid_6708701
GTPL13081
3a,7a-Dimethylhexahydro-4,7-epoxyisobenzofuran-1,3-dione
HMS2097B12
HMS3412J13
HMS3676J13
1,6-epoxyperhydrophthalic anhydride
4,7-Epoxyisobenzofuran-1,3-dione, hexahydro-3a,7a-dimethyl-, (3a.alpha.,4.beta.,7.beta.,7a.alpha.)-
BCP09819
HY-N0209
BDBM50090505
CCG-35382
CCG-36082
WHO 11470
AKOS015895930
AC-7967
CS-4979
DB12328
FC29633
4,3-dione, hexahydro-3a,7a-dimethyl-
exo-1,6-epoxyhexahydrophthalic anhydride
NCGC00025212-02
NCGC00025212-03
NCGC00025212-04
NCGC00025212-05
NCGC00025212-31
1ST40063
AS-18735
NCI60_005413
VP-102 drug/device delivering cantharidin
WLN: T C555 A AO DVOVTJ C1 G1
AB00513946
Hexahydro-3a,7-epoxyisobenzofuran-1,3-dione
D11745
7-Oxabicyclo[2.2.1]heptane-2, 2,3-dimethyl-
EN300-24727854
Q410884
SR-01000597585
SR-01000597585-1
BRD-K80684056-001-01-0
BRD-K80684056-001-04-4
BRD-K80684056-001-05-1
BRD-K80684056-001-06-9
Hexahydro-3a,7a-dimethyl-4,7-epoxyisobenzo-furan-1,3-dione
(3aR,4S,7R,7aS)-3a,7a-dimethylhexahydro-4,7-epoxyisobenzofuran-1,3-dione
(1R,2S,6R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione
(1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.0,2,6]decane-3,5-dione
(1R,2S,6R,7S)-2,6-dimethyl-4,10-dioxatricyclo[5.2.1.02,6]decane-3,5-dione
(1R,7S)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione
(1S,2R,6S,7R)-2,6-Dimethyl-4,10-dioxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione
(1S,3S,4R,7R)-2,6-dimethyl-4,10-dioxa-tricyclo[5.2.1.0-2,6]decane-3,5-dione
4,3-dione, hexahydro-3a,7a-dimethyl-, (3a.alpha.,4.beta.,7.beta.,7a.alpha.)-
4,7-EPOXYISOBENZOFURAN-1.3-DIONE, HEXAHYDRO-3a,7a-DIMETHYL-, (3aR,4S,7R,7aS)-REL-
HEXAHYDRO-3A ALPHA, 7A ALPHA-DIMETHYL-4 BETA, 7 BETA-EPOXYISOBENZOFURAN-1,3-DIONE
200-263-3
4,7-EPOXYISOBENZOFURAN-1,3-DIONE, HEXAHYDRO-3A,7A-DIMETHYL-,(3A ALPHA, 4 BETA, 7 BETA, 7A ALPHA)-
Cantharidine; 3a,7a-Dimethylhexahydro-4,7-epoxyisobenzofuran-1,3-dione; 7a-Dimethylhexahydro-3a,4,7-epoxyisobenzofuran