Interesting facts
Interesting Facts about 1-Chloropyrrolidine-2,5-dione
1-Chloropyrrolidine-2,5-dione is a fascinating compound that piques the interest of chemists due to its unique structural features and versatile applications. Here are some key highlights:
- Structural Significance: This compound contains a pyrrolidine ring, which is a five-membered nitrogen-containing heterocycle. The presence of a chlorine atom adds to its reactivity, making it a subject of extensive research in synthetic chemistry.
- Potential Applications: 1-Chloropyrrolidine-2,5-dione has potential applications in various fields, including medicinal chemistry. Derivatives of this compound may exhibit interesting biological activities, which could be beneficial in drug discovery.
- Versatile Reagent: As a chlorinated compound, it can serve as a versatile reagent in organic synthesis, facilitating the formation of various other organic compounds through nucleophilic substitution reactions.
- Research Interest: This compound is often studied for its role in the synthesis of amino acid derivatives and other biologically relevant molecules, highlighting its importance in the pharmaceutical industry.
- Chirality Considerations: The presence of the pyrrolidine moiety also raises intriguing questions around chirality and enantiomeric purity, which are critical for the development of effective medications.
In summary, 1-chloropyrrolidine-2,5-dione is not just another chemical compound; it's a gateway to advanced research and a potential key player in future therapeutic agents. As a chemistry student or researcher, exploring its properties and applications could lead to exciting discoveries in the realm of organic and medicinal chemistry.
Synonyms
N-CHLOROSUCCINIMIDE
128-09-6
1-chloropyrrolidine-2,5-dione
Succinchlorimide
Chlorosuccinimide
Succinochlorimide
2,5-Pyrrolidinedione, 1-chloro-
Succinic N-chloroimide
1-Chloro-2,5-pyrrolidinedione
Succinic acid, imide, N-chloro-
NSC-8748
0FWP306H7X
DTXSID2042199
CHEBI:53203
DTXCID0022199
RefChem:163119
204-878-8
Succinimide, N-chloro-
NCS
C4H4ClNO2
MFCD00005511
NSC 8748
1-Chloro-2,5-pyrrolidine-dione
1-chloroazolidine-2,5-dione
Caswell No. 807
N-chloro-succinimide
N-Chloro succinimide
HSDB 5407
Succinchlorimide [NF]
EINECS 204-878-8
EPA Pesticide Chemical Code 077301
BRN 0113915
UNII-0FWP306H7X
AI3-52304
n-chlorsuccinimide
n-chorosuccinimide
N-chlorosuccinimid
N-chlorosucinimide
N-Clorosuccinimide
N-chlorosuccinirnide
N -chlorosuccinimide
N-chlorosuc-cinimide
N-Chlorosuccinimid e
2, 1-chloro-
SCHEMBL72
WLN: T5VNVTJ BG
N-chlorosuccinic acid imide
N-Chlorosuccinimide, 98%
5-21-09-00543 (Beilstein Handbook Reference)
SUCCINCHLORIMIDE [HSDB]
1-chloro-2,5 pyrrolidinedione
orb2664355
SCHEMBL5897812
SCHEMBL8158051
CHEMBL2107513
N-CHLOROSUCCINIMIDE [MI]
SUCCINCHLORIMIDE [MART.]
1-chloro-pyrrolidine-2,5-dione
NSC8748
1-chloro-pyrrolidine-2, 5-dione
BCP27379
HY-Y0532
Tox21_301368
BBL027530
SBB058749
STL194270
AKOS000121131
FC14779
PS-3219
NCGC00255991-01
BP-21326
CAS-128-09-6
DB-007755
NS00006599
ST51037890
EN300-25969
D78048
F005014
Q286192
F0001-0394
InChI=1/C4H4ClNO2/c5-6-3(7)1-2-4(6)8/h1-2H
Solubility of 1-Chloropyrrolidine-2,5-dione
1-Chloropyrrolidine-2,5-dione is an intriguing compound that presents unique solubility characteristics. Understanding its solubility behavior can enhance its application in various chemical processes. Here are some key points regarding its solubility:
In conclusion, the solubility of 1-chloropyrrolidine-2,5-dione is determined by factors such as solvent choice, temperature, and its unique molecular structure. As one might say, “The ability to dissolve reveals much about a compound’s potential.” Thus, exploring its solubility is crucial for optimizing its applications in chemical synthesis and formulation.