Interesting facts
Interesting Facts about 1,3-Dicyclohexylurea
1,3-Dicyclohexylurea is an intriguing compound that combines elements of organic chemistry with practical applications. Here are some notable points about this fascinating compound:
- Structure and Functionality: The structure of 1,3-dicyclohexylurea features two cyclohexyl groups attached to a urea backbone. This unique molecular design contributes to its properties and potential applications in various chemical reactions.
- Synthesis: 1,3-Dicyclohexylurea can be synthesized from the reaction of cyclohexyl isocyanate and an amine. The process showcases the beauty of synthetic organic chemistry, highlighting the importance of reaction conditions and reagent selection.
- Stabilizing Agent: This compound functions as a stabilizing agent in numerous chemical processes, particularly in the realm of catalysis. Its ability to stabilize transition states makes it an invaluable resource for chemists looking to optimize reactions.
- Use in Chemistry: Known for its role in facilitating the formation of certain types of chemical bonds, 1,3-dicyclohexylurea has been explored for its applications in material science and organic synthesis.
- Thermal and Chemical Stability: The stability of this compound under various conditions allows for its utilization in both academic and industry settings. Its robustness is a crucial factor in experimental methods.
As a graduate student or a researcher in the field of chemistry, understanding the role of compounds like 1,3-dicyclohexylurea can expand your knowledge base and enhance your experimentation toolkit. It exemplifies the combination of structure and function, serving as a reminder of how creative chemistry can solve real-world challenges.
Synonyms
1,3-Dicyclohexylurea
n,n'-dicyclohexylurea
2387-23-7
Dicyclohexylurea
Urea, N,N'-dicyclohexyl-
Urea, 1,3-dicyclohexyl-
MFCD00003829
ZV7823VVIM
EINECS 219-213-7
NSC 17013
NSC 30023
NSC-17013
NSC-30023
CHEMBL1458
DICYCLOHEXYLCARBODIAMIDE
DICYCLOHEXYLUREA, N,N'-
Urea,3-dicyclohexyl-
Urea,N'-dicyclohexyl-
LOMUSTINE IMPURITY C [EP IMPURITY]
DCU compound
LOMUSTINE IMPURITY C (EP IMPURITY)
C13H24N2O
UNII-ZV7823VVIM
dicylohexylurea
dicylcohexylurea
dicylohexyl urea
dicyclohexyl urea
dicyclohexyl-urea
N,N inverted exclamation marka-Dicyclohexylurea
DCW
1,3dicyclohexylurea
n.n'-dicyclohexylurea
N,N,-Dicyclohexylurea
1,3-dicyclohexyl-urea
Urea, 1,3dicyclohexyl
N,N'-dicyclohexyl urea
Urea, N,N'dicyclohexyl
N,N'-dicyclohexylisourea
1,3-dicyclo hexyl urea
N.N' - dicyclohexylurea
Urea-based compound, 12
SCHEMBL2755
Oprea1_447813
SPECTRUM1505126
N,N'-Dicyclohexylurea, 98%
F0902-7614
DTXSID3062366
SCHEMBL14602374
Urea, 1,3dicyclohexyl (8CI)
BDBM25731
CHEBI:93429
1,3-Dicyclohexylurea (Standard)
Urea, 1,3-dicyclohexyl-(8CI)
HY-W013989R
NSC17013
NSC30023
HSCI1_000378
STK093362
US8815951, 1,3-dicyclohexylurea
AKOS000121544
AB10257
CCG-214823
CS-W014705
HY-W013989
NCGC00095983-01
AS-57476
SY049014
DB-046275
D0441
EU-0099846
NS00010594
EN300-15666
SR-01000596919
Q5274028
SR-01000596919-1
BRD-K81521265-001-01-0
BRD-K81521265-001-02-8
Z44585884
219-213-7
DHU
Solubility of 1,3-dicyclohexylurea
1,3-dicyclohexylurea (C13H24N2O) exhibits unique solubility characteristics that are worth noting. This compound demonstrates limited solubility in water, which is common for urea derivatives featuring bulky cycloalkane structures. The presence of the two cyclohexyl groups contributes significantly to its hydrophobic nature.
Key points to consider about its solubility include:
In conclusion, while 1,3-dicyclohexylurea’s solubility in water is limited, its solubility in organic solvents is favorable, opening avenues for various chemical reactions and formulations. Understanding these solubility properties is essential for effectively utilizing this compound in synthetic chemistry.