Cas no 19757-64-3 (cyclopropylurea)
cyclopropylurea Chemical and Physical Properties
Names and Identifiers
-
- Urea,N-cyclopropyl-
- cyclopropylurea
- N-CYCLOPROPYLUREA
- 1-cyclopropylurea
- AC1L6S21
- AC1Q4ZW4
- AC1Q5JFX
- Cyclopropylharnstoff
- Cyclopropyl-harnstoff
- cyclopropyl-urea
- N-Cyclopropyl-harnstoff
- NSC117244
- SureCN687674
- (Carbamoylamino)cyclopropane, Ureidocyclopropane
- Z57000532
- Urea, N-cyclopropyl-
- BS-12686
- NSC-117244
- SCHEMBL687674
- DTXSID00297670
- CS-0073680
- cyclopropyl urea
- F8880-2529
- 19757-64-3
- CLMGCKCDSPUQEE-UHFFFAOYSA-N
- AKOS000200343
- MFCD01569844
- EN300-13158
- D73868
- DB-244326
-
- MDL: MFCD01569844
- Inchi: 1S/C4H8N2O/c5-4(7)6-3-1-2-3/h3H,1-2H2,(H3,5,6,7)
- InChI Key: CLMGCKCDSPUQEE-UHFFFAOYSA-N
- SMILES: O=C(N)NC1CC1
Computed Properties
- Exact Mass: 100.06374
- Monoisotopic Mass: 100.064
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 7
- Rotatable Bond Count: 1
- Complexity: 87.7
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: -0.5
- Topological Polar Surface Area: 55.1?2
Experimental Properties
- Density: 1.17
- Melting Point: 123-124 °C
- Boiling Point: 179.7°Cat760mmHg
- Flash Point: 62.5°C
- Refractive Index: 1.519
- PSA: 55.12
cyclopropylurea Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Chemenu | CM350034-1g |
1-Cyclopropylurea |
19757-64-3 | 95%+ | 1g |
$258 | 2023-02-17 | |
| Chemenu | CM350034-5g |
1-Cyclopropylurea |
19757-64-3 | 95%+ | 5g |
$1049 | 2022-09-01 | |
| Chemenu | CM350034-10g |
1-Cyclopropylurea |
19757-64-3 | 95%+ | 10g |
$1558 | 2022-09-01 | |
| Apollo Scientific | OR21332-250mg |
1-Cyclopropylurea |
19757-64-3 | 96% | 250mg |
£53.00 | 2025-02-19 | |
| Apollo Scientific | OR21332-1g |
1-Cyclopropylurea |
19757-64-3 | 96% | 1g |
£121.00 | 2025-02-19 | |
| abcr | AB238391-250 mg |
N-Cyclopropylurea; . |
19757-64-3 | 250 mg |
€186.50 | 2023-07-20 | ||
| abcr | AB238391-1 g |
N-Cyclopropylurea; . |
19757-64-3 | 1 g |
€441.50 | 2023-07-20 | ||
| eNovation Chemicals LLC | Y1238961-1g |
Urea, N-cyclopropyl- |
19757-64-3 | 97% | 1g |
$135 | 2024-06-07 | |
| abcr | AB238391-5 g |
N-Cyclopropylurea; . |
19757-64-3 | 5 g |
€1,257.50 | 2023-07-20 | ||
| Chemenu | CM350034-100mg |
1-Cyclopropylurea |
19757-64-3 | 95%+ | 100mg |
$51 | 2023-02-17 |
cyclopropylurea Suppliers
cyclopropylurea Related Literature
-
Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
-
Nan Fu,Naphaporn Chiewchan,Xiao Dong Chen Food Funct., 2020,11, 211-220
-
Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
-
Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
Additional information on cyclopropylurea
Cyclopropylurea: A Comprehensive Overview
Cyclopropylurea, also known by its CAS number 19757-64-3, is a chemical compound that has garnered significant attention in various scientific and industrial applications. This compound is a derivative of urea, with a cyclopropyl group attached, making it unique in terms of its chemical structure and properties. The cyclopropylurea molecule is characterized by its ability to form hydrogen bonds, which contributes to its versatility in different chemical reactions and applications.
Recent studies have highlighted the potential of cyclopropylurea in the field of medicinal chemistry. Researchers have explored its role as a building block for the synthesis of bioactive compounds, particularly in the development of new drug candidates. The compound's ability to act as a template for assembling complex molecular architectures has made it a valuable tool in drug design. For instance, cyclopropylurea derivatives have been investigated for their potential as inhibitors of certain enzymes, which could lead to novel therapeutic agents.
In addition to its role in drug discovery, cyclopropylurea has also found applications in materials science. Its unique chemical properties make it an ideal candidate for the synthesis of advanced materials, such as polymers and coatings. Recent advancements in polymer chemistry have demonstrated that cyclopropylurea can be used to create materials with enhanced mechanical and thermal stability. These materials hold promise for use in high-performance applications, such as aerospace and automotive industries.
The synthesis of cyclopropylurea involves a multi-step process that typically begins with the reaction of cyclopropane derivatives with urea precursors. This process requires precise control over reaction conditions to ensure high yields and purity. Recent research has focused on optimizing these synthesis methods to make them more efficient and environmentally friendly. For example, the use of catalytic systems and green chemistry principles has been explored to reduce waste and energy consumption during the production of cyclopropylurea.
Another area where cyclopropylurea has shown potential is in agrochemicals. Its ability to interact with biological systems makes it a candidate for the development of pesticides and herbicides. However, extensive testing is required to ensure that these applications are safe for both human health and the environment. Researchers are currently investigating the environmental fate and toxicity of cyclopropylurea derivatives to assess their suitability for agricultural use.
From a structural standpoint, cyclopropylurea exhibits interesting properties due to the strained ring system of the cyclopropane group. This strain can lead to unique reactivity patterns, which have been exploited in various organic transformations. For instance, the compound has been used as a substrate in cycloaddition reactions, which are fundamental processes in organic chemistry. These reactions have enabled the construction of complex molecules with high precision.
Moreover, cyclopropylurea has been studied for its potential in catalysis. Its ability to coordinate with metal ions makes it a promising candidate for designing catalysts with high activity and selectivity. Recent research has focused on using cyclopropylurea as a ligand in transition metal complexes, which could find applications in industrial catalysis processes such as olefin polymerization and hydrogenation.
In terms of spectroscopic analysis, cyclopropylurea exhibits distinct absorption bands that make it amenable to various analytical techniques. Techniques such as infrared spectroscopy (IR), nuclear magnetic resonance (NMR), and mass spectrometry (MS) have been employed to characterize its structure and purity. These analyses are crucial for ensuring the quality of cyclopropylurea products used in research and industrial settings.
The global demand for compounds like cyclopropylurea is driven by their versatility across multiple industries. As research continues to uncover new applications and improve existing ones, the significance of this compound is expected to grow further. Its role in advancing fields such as drug discovery, materials science, and catalysis underscores its importance as a key player in modern chemistry.