Interesting facts
Interesting Facts about 2-amino-3-chloro-naphthalene-1,4-dione
2-amino-3-chloro-naphthalene-1,4-dione is a fascinating compound that belongs to the class of naphthoquinone derivatives. Here are some captivating insights:
- Diverse Applications: This compound is utilized in various fields such as organic synthesis, pharmaceuticals, and dyes. Its derivatives often possess valuable biological activities, making them important in medicinal chemistry.
- Structural Significance: The presence of both amino and chloro groups in its structure contributes to its reactivity and interaction with various biological systems. The arrangement of atoms in the naphthalene ring allows for interesting electronic properties.
- Biological Activity: Compounds like 2-amino-3-chloro-naphthalene-1,4-dione exhibit potential antimicrobial and cytotoxic activities. Research continues to explore these properties, aiming at developing new therapeutic agents.
- Synthetic Pathways: The synthesis of this compound typically involves multi-step reactions, starting with naphthalene and incorporating chlorination and amination processes. This complexity can be both a challenge and an opportunity for chemists looking to innovate.
- Color Chemistry: Due to the presence of naphthoquinone in its structure, this compound may participate in color-forming reactions that can be exploited in the dye industry. Its vibrant hues are appealing in various applications.
This compound not only showcases the intricate world of organic chemistry but also highlights the ongoing potential for new discoveries in therapeutic and industrial applications. As research uncovers more about its properties and functions, 2-amino-3-chloro-naphthalene-1,4-dione stands as a testament to the diversity of chemical compounds.
Synonyms
2797-51-5
Quinoclamine
2-Amino-3-chloro-1,4-naphthoquinone
2-amino-3-chloronaphthalene-1,4-dione
Mogeton
06K-Quinone
O 6K-quinone
Mogeton granule
Mogeton G
1,4-Naphthalenedione, 2-amino-3-chloro-
Quinoclamine [ISO]
NSC 3910
2-Amino-3-chloronaphthoquinone
1,4-Naphthoquinone, 2-amino-3-chloro-
06K-50W
NSC 642009
EINECS 220-529-2
JN6NK7K14F
BRN 2094762
NSC-3910
QUINOCLAMINE [MI]
NSC-642009
DTXSID1041390
2-AMINO-3-CHLORO-1,4-NAPHTHALENEDIONE
2-ACl-NQ
DTXCID9021390
220-529-2
Quinoclamin
ACNQ
2-Chloro-3-amino-1,4-naphthoquinone
MFCD00001680
06K
2-amino-3-chloro-1,4-dihydronaphthalene-1,4-dione
MLS002701536
CHEBI:81849
NSC3910
NSC642009
Quinoclamine 100 microg/mL in Acetone
UNII-JN6NK7K14F
2-Amino-3-chloro-[1,4]naphthoquinone
Quinoclamine (Standard)
1, 2-amino-3-chloro-
SCHEMBL119489
Quinoclamine pound>>Quinoclamin
CHEMBL156959
OBLNWSCLAYSJJR-UHFFFAOYSA-
WLN: L66 BV EVJ CZ DG
BCP21702
CAA79751
DNDI1416924
STK260051
3-Chloro-2-amino-1,4-naphthoquinone
AKOS000108631
DS-0569
HY-121632R
RTI1218-1-1
2-amino-3-chloro-naphthalene-1,4-dione
NCI60_014211
SMR001565137
SY047011
DB-080905
HY-121632
2-azanyl-3-chloranyl-naphthalene-1,4-dione
A1288
CS-0082921
NS00006275
EN300-29644
C18584
E78086
Quinoclamine, PESTANAL(R), analytical standard
A819269
2-amino-3-chloro-1,4-dihydro-1,4-dioxonaphthalene
Q2123248
2-amino-3-chloro-1,4-dihydro-1,4-dioxo-naphthalene
Z57178974
InChI=1/C10H6ClNO2/c11-7-8(12)10(14)6-4-2-1-3-5(6)9(7)13/h1-4H,12H2
Butanedioic acid,4-dihydro-1,4-dioxo- 2-naphthalenyl)amino]1,2-dioxo]ethyl]-3-oxo-, dimethyl ester
Solubility of 2-amino-3-chloro-naphthalene-1,4-dione
2-amino-3-chloro-naphthalene-1,4-dione, often referred to in scientific contexts for its unique structure, exhibits certain characteristics concerning its solubility:
In essence, one might consider that the solubility of 2-amino-3-chloro-naphthalene-1,4-dione is influenced significantly by its functional groups, with important implications for its behavior in various chemical environments.