Interesting facts
Interesting Facts About 1,3-benzoxazine-2,4-dione
1,3-benzoxazine-2,4-dione, often recognized for its unique bicyclic structure, belongs to a class of organic compounds that has garnered significant attention in the fields of organic chemistry and materials science.
Chemical Properties and Applications
This compound is known for:
- Versatile Reactivity: It can participate in various chemical reactions, making it a valuable intermediate in organic synthesis.
- Biological Activity: Some derivatives of 1,3-benzoxazine-2,4-dione have demonstrated potential as anti-cancer agents and anti-inflammatory agents, showcasing its importance in medicinal chemistry.
- Material Science: The compound has promising applications in polymer chemistry, particularly in developing new materials with desired thermal and mechanical properties.
Unique Structural Features
The distinct structure of 1,3-benzoxazine-2,4-dione contributes to its intriguing properties:
- Heterocyclic Ring System: The presence of both carbon and oxygen atoms in the ring system enhances its chemical stability.
- Position of Functional Groups: The positioning of the carbonyl groups affects its reactivity and interaction with other chemical species.
Environmental and Safety Considerations
As with many chemical compounds, handling 1,3-benzoxazine-2,4-dione safely is crucial. Proper laboratory practices should be followed to mitigate any health risks associated with its use.
In summary, 1,3-benzoxazine-2,4-dione serves as an excellent example of how a simple molecule can have diverse applications in various scientific domains. Its rich chemistry continues to inspire research and innovation.
Synonyms
Carsalam
2037-95-8
2H-1,3-BENZOXAZINE-2,4(3H)-DIONE
Beaprine
1,3-Benzoxazine-2,4-dione
Ruhmal
Oxophenhydroxazine
Oxobenzhydroxazin
Oxophenhydroxazin
Carsalamo
Carsalamum
Carsalamum [INN-Latin]
Carsalamo [INN-Spanish]
Carsalam [INN:BAN:DCF]
NSC 36166
NSC-36166
4H-1,3-Benzoxazine-2,4(3H)-dione
BRN 0136767
DTXSID3046584
OXYPHENHYDRAZINE
AI3-25161
685H843ULU
CARSALAM [INN]
CARSALAM [MI]
DTXCID1026584
4-27-00-03326 (Beilstein Handbook Reference)
Carsalamum (INN-Latin)
Carsalamo (INN-Spanish)
2H-1,3-benzoxazin-4(3H)-one
606-541-4
2H-Benzo[e][1,3]oxazine-2,4(3H)-dione
3,4-dihydro-2H-1,3-benzoxazine-2,4-dione
MFCD00600566
NCGC00166265-01
CAS-2037-95-8
SR-01000392668
UNII-685H843ULU
2H-1,4(3H)-dione
4H-1,4(3H)-dione
SCHEMBL26521
MLS001249437
CHEMBL1720051
SCHEMBL17844931
CHEBI:134794
HMS3264N17
Pharmakon1600-01504504
HY-B1047
NSC36166
Tox21 112383
Tox21_112383
NSC758885
s4555
AKOS015917497
Tox21_112383_1
CCG-213935
CS-4568
FB45734
FD10735
NSC-758885
NCGC00166265-02
AS-10042
DA-51595
SMR000718659
SY110608
SBI-0207074.P001
2-hydroxy-4h-benzo[e][1,3]oxazin-4-one
4-hydroxy-2h-benzo[e][1,3]oxazin-2-one
EU-0067206
NS00026608
2H-1,3-Benzoxazine-2,4(3H)-dione, 98%
EN300-330999
AB00632416_03
AJ-333/25006179
SR-01000392668-1
SR-01000392668-2
BRD-K13238618-001-01-8
BRD-K13238618-001-05-9
Q27264215
Z1255365144
InChI=1/C8H5NO3/c10-7-5-3-1-2-4-6(5)12-8(11)9-7/h1-4H,(H,9,10,11
J9W
Solubility of 1,3-benzoxazine-2,4-dione
1,3-benzoxazine-2,4-dione, often encountered in various chemical and therapeutic applications, displays specific solubility characteristics that are noteworthy:
As with many organic compounds, factors such as temperature, pressure, and molecular structure play crucial roles in determining solubility. It's essential to consider these factors when attempting to dissolve 1,3-benzoxazine-2,4-dione in different environments.
Understanding the solubility behavior of 1,3-benzoxazine-2,4-dione is vital for its effective utilization in various chemical processes and applications.