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Sericealactone A

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Identification
Molecular formula
C21H26O3
CAS number
155589-79-6
IUPAC name
(4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione
State
State

At room temperature, Sericealactone A exists as a solid.

Melting point (Celsius)
179.50
Melting point (Kelvin)
452.65
Boiling point (Celsius)
535.10
Boiling point (Kelvin)
808.25
General information
Molecular weight
346.41g/mol
Molar mass
346.4130g/mol
Density
1.2100g/cm3
Appearence

Sericealactone A is observed as a light yellow solid. The structure can be crystalline under certain conditions, reflecting light with a subtle shine.

Comment on solubility

Solubility of (4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione

The solubility of complex organic compounds like (4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione can be influenced by various factors:

  • Polarity: The presence of functional groups and their arrangement can lead to variations in polarity, affecting solubility in polar versus non-polar solvents.
  • Hydrogen Bonding: Compounds capable of forming hydrogen bonds typically exhibit increased solubility in polar solvents, such as water.
  • Molecular Weight: Higher molecular weights can hinder solubility; however, some larger molecules still dissolve well in specific solvents.
  • Temperature: Increasing temperature generally enhances solubility for most solids due to increased molecular motion.
  • Interactions: Specific interactions with solvent molecules, including van der Waals forces, can also dictate solubility characteristics.

For this particular compound, empirical data is essential to ascertain its exact solubility properties. If you were to test its solubility, it might reveal that:

  • It is soluble in organic solvents like ethanol or dimethyl sulfoxide (DMSO).
  • It may have limited solubility in water due to its likely non-polar characteristics.

Understanding these factors and their influences on solubility not only aids in practical applications but also enhances our comprehension of the compound's behavior in various environments.

Interesting facts

Interesting Facts about (4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione

This compound, belonging to the chemical family of naphthoquinones, is notable for its unique structure and potential applications in various fields. Its complex stereochemistry plays a significant role in determining its biological activity and interactions. Here are some intriguing aspects of this compound:

  • Structural Complexity: The intricate arrangement of atoms in the compound contributes to its rich chemical properties. The multiple fused rings not only enhance its stability but also influence reactivity patterns.
  • Biological Relevance: Compounds similar to this one have been researched for their roles in medicinal chemistry. They are often investigated for their potential as anticancer agents, highlighting the importance of understanding their mechanisms of action.
  • Natural Occurrence: Naphthoquinones are often found in various natural sources, including plants and fungi. This compound may share similarities with naturally occurring compounds, pointing to fascinating biogenic routes.
  • Applications in Organic Synthesis: The unique properties of this compound make it an interesting target for synthetic chemists, who may use it as a building block for creating more complex molecules.
  • Research Potential: Ongoing studies into the applications of this compound in areas such as photochemistry and material science continue to unveil its potential, making it a topic of significant interest in contemporary chemistry.

As a final thought, the study of such complex compounds not only enriches our understanding of chemistry but also facilitates the discovery of new avenues for research and application.

Synonyms
testolactone
968-93-4
Teolit
Fludestrin
Testolacton
1-Dehydrotestololactone
delta(1)-Testololactone
1,2-Didehydrotestololactone
Testolactona
Testolactonum
Testolattone
Testolactonum [INN-Latin]
Testolactona [INN-Spanish]
D-Homo-17A-oxaandrosta-1,4-diene-3,17-dione
SQ 9538
Testololactone, 1-dehydro-
SQ-9538
delta(1)-Dehydrotestolactone
Testolactone ciii
13-Hydroxy-3-oxo-13,17-secoandrosta-1,4-dien-17-oic acid delta-lactone
delta1-Testololactone
Teslak
NSC-23759
Delta-1-testololactone
Testololactone, 1,2-didehydro-
HSDB 3255
1,2-Dehydrotestololactone
EINECS 213-534-6
UNII-6J9BLA949Q
NSC 23759
6J9BLA949Q
CHEBI:9460
17alpha-Oxo-D-homo-1,4-androstadiene-3,17-dione
DTXSID2023644
therapeutic testolactone
3-oxo-13,17-secoandrosta-1,4-dieno-17,13alpha-lactone
(4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2H-naphtho[2,1-f]chromene-2,8(4bH)-dione
DTXCID303644
Testolactone [USAN:USP:INN]
1,2,3,4,4a,4b,7,9,10,10a-Decahydro-2-hydroxy-2,4b-dimethyl-7-oxo-1-phenanthrenepropionic acid delta-lactone
NSC23759
13,17-Secoandrosta-1,4-dien-17-oic acid, 13-hydroxy-3-oxo-, delta-lactone
delta(1)-Testolactone
Testolactonum (INN-Latin)
Testolactona (INN-Spanish)
TESTOLACTONE (USP-RS)
TESTOLACTONE [USP-RS]
Testolactone (USAN:USP:INN)
1 Dehydrotestolactone
1-Dehydrotestolactone
TESTOLACTONE (USP IMPURITY)
TESTOLACTONE [USP IMPURITY]
TESTOLACTONE CIII (USP-RS)
TESTOLACTONE CIII [USP-RS]
(4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-3,4,4a,5,6,10a,10b,11,12,12a-decahydro-2H-naphtho(2,1-f)chromene-2,8(4bH)-dione
DELTA(1)-DEHYDROTESTOLOLACTONE
13-Hydroxy-3-0x0-13,17-secoandrosta-1,4-dien-17-oic Acid Delta-Lactone
213-534-6
nsc-12173
Teslac
Testolattone [DCIT]
(4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10b,11,12-octahydro-3H-naphtho[2,1-f]chromene-2,8-dione
NSC 12173
(4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-4,4a,4b,5,6,10a,10b,11,12,12a-decahydro-2H-naphtho[2,1-f]chromene-2,8(3H)-dione
.DELTA.1-Testololactone
.DELTA.1-Dehydrotestolactone
TESLAC (TN)
Testolactone (USP/INN)
.DELTA.1-Dehydrotestololactone
NCGC00159329-02
Delta1-Testolactone
TESTOLACTONE [MI]
TESTOLACTONE [INN]
TESTOLACTONE [HSDB]
TESTOLACTONE [USAN]
SCHEMBL4053
Testololactone,2-didehydro-
CHEMBL1571
TESTOLACTONE [VANDF]
TESTOLACTONE [WHO-DD]
GTPL7303
BPEWUONYVDABNZ-DZBHQSCQSA-N
HMS3750O07
TESTOLACTONE [ORANGE BOOK]
BCP10926
Tox21_111576
BDBM50367848
LMST02020084
17a-Oxa-D-homoandrosta-1,17-dione
D-Homo-17a-oxaandrosta-1,17-dione
AKOS015840139
CS-5268
DB00894
CAS-968-93-4
HY-13763
NCI60_001908
NS00004469
C02197
D00153
Q3985253
BRD-K69636617-001-01-7
13,4-dien-17-oic acid, 13-hydroxy-3-oxo-, lactone
13-Hydroxy-3-oxo-13,4-dien-17-oic acid .delta.-lactone
13,4-dien-17-oic acid, 13-hydroxy-3-oxo-, .delta.-lactone
13-Hydroxy-3-oxo-13,17-secoandrosta-1,4-dien-17-oic acid lactone
13,4-dien-17-oic acid, 13.alpha.-hydroxy-3-oxo-, .delta.-lactone
2H-Phenanthro[2,8(4bH)-dione, 3,4,4a,5,6,10a,10b,11,12,12a-decahydro-10a,12a-dimethyl-, lactone