Interesting facts
Interesting Facts About 1-Cyclohexyl-3-(p-tolylsulfonyl)urea
1-Cyclohexyl-3-(p-tolylsulfonyl)urea, often recognized in the field of organic chemistry for its unique structure and applications, is a fascinating compound with a variety of interesting properties and uses.
Key Points of Interest:
- Synthesis: This compound is typically synthesized through a series of reactions involving cyclohexyl amine and p-tolylsulfonyl isocyanate. Its formation is a great example of how functional groups can influence molecular properties.
- Biological Activity: Research has indicated that compounds like 1-cyclohexyl-3-(p-tolylsulfonyl)urea exhibit interesting biological activities, making them candidates for pharmaceuticals, particularly in anti-inflammatory and analgesic therapies.
- Applications: Beyond medicinal uses, this compound can also be utilized in agricultural chemistry, serving as a herbicide or pesticide in certain formulations, thus showcasing its versatility in chemical applications.
- Structure-Activity Relationship: The presence of both the cyclohexyl group and the p-tolylsulfonyl moiety contributes significantly to the compound's properties. Understanding how these groups interact at the molecular level is crucial for the design of new derivatives.
In conclusion, 1-cyclohexyl-3-(p-tolylsulfonyl)urea is not just a compound with a complex name; it is a representative of the intricate interplay between structure and function in medicinal chemistry. As one researcher noted, "The confluence of various functional groups in organic synthesis opens endless possibilities for innovation."
Synonyms
Glycyclamide
TOLCYCLAMIDE
664-95-9
Cychloral
Cyclamid
Gliciclamide
Glycyclamid
Tolhexamide
Agliral
Glicosil
Gliciclamida
Glycyclamide [INN]
Glycyclamidum
Gliciclamide [DCIT]
1-Cyclohexyl-3-p-tolylsulfonylurea
Glycyclamidum [INN-Latin]
Gliciclamida [INN-Spanish]
1-Cyclohexyl-3-p-toluenesulfonylurea
1-(p-Tolylsulfonyl)-3-cyclohexylurea
N-Cyclohexyl-N'-(p-tolylsulfonyl)urea
N-(4-Tolylsulfonyl)-N'-cyclohexylurea
Urea, 1-cyclohexyl-3-(p-tolylsulfonyl)-
K 386
K-386
EINECS 211-557-6
UNII-C40N4EJY68
N-(4-Methylbenzenesulfonyl)-N'-cyclohexylurea
NSC 142661
NSC-142661
BRN 1995860
Glycyclamide (INN)
DTXSID5046273
1-Cicloesil-3-p-tolilsolfonilurea
1-Cicloesil-3-p-tolilsolfonilurea [Italian]
TOLCYCLAMIDE [MI]
GLYCYCLAMIDE [MART.]
GLYCYCLAMIDE [WHO-DD]
Benzenesulfonamide, N-((cyclohexylamino)carbonyl)-4-methyl-
DTXCID3026273
4-12-00-00057 (Beilstein Handbook Reference)
Glycyclamidum (INN-Latin)
Gliciclamida (INN-Spanish)
GLYCYCLAMIDE (MART.)
Benzenesulfonamide, N-[(cyclohexylamino)carbonyl]-4-methyl-
1-cyclohexyl-3-tosylurea
Diabomet
Diaborale
1-Cyclohexyl-3-p-tolylsulphonylurea
1-cyclohexyl-3-(p-toluenesulfonyl)urea
Benzenesulfonamide, N-((cyclohexylamino)carbonyl)-4-methyl-(9CI)
211-557-6
cicloral
Cyclamide
1-cyclohexyl-3-(4-methylphenyl)sulfonylurea
K-38
C40N4EJY68
NCGC00160649-01
N-(cyclohexylcarbamoyl)-4-methylbenzenesulfonamide
Cyclamide [Russian]
CAS-664-95-9
SR-01000945146
Tolcyclamide K 38
Oprea1_220838
Oprea1_641283
SCHEMBL49386
WLN: L6TJ AMVMSWR D1
CHEMBL312394
N-[(Cyclohexylamino)carbonyl]-4-methylbenzenesulfonamide
SCHEMBL19925500
CHEBI:135251
RIGBPMDIGYBTBJ-UHFFFAOYSA-N
Tox21_111956
GS4037
NSC142661
STK041315
AKOS001218044
Tox21_111956_1
CCG-357214
NCGC00160649-02
DS-010299
HY-119982
CS-0078864
NS00036043
D02426
SR-01000945146-1
SR-01000945146-2
Q17631916
Z44585883
Benzenesulfonamide,n-[(cyclohexylamino)carbonyl]-4-methyl-
Solubility of 1-cyclohexyl-3-(p-tolylsulfonyl)urea
The compound 1-cyclohexyl-3-(p-tolylsulfonyl)urea exhibits unique solubility characteristics due to its specific molecular structure. This urea derivative is known to have varying solubility in different solvents:
It's crucial to note that factors such as temperature, solvent polarity, and intermolecular interactions play significant roles in determining the solubility of 1-cyclohexyl-3-(p-tolylsulfonyl)urea. As a general observation:
Always consider these elements when evaluating the solubility of this compound in various conditions.