Cas no 556-10-5 ((4-Nitrophenyl)urea)
(4-Nitrophenyl)urea Chemical and Physical Properties
Names and Identifiers
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- (4-Nitrophenyl)urea
- 4-Nitrophenylurea
- AC1L7NM6
- AC1Q4ZV9
- ENT 61327
- N-(4-nitrophenyl)urea
- N-(p-nitrophenyl)urea
- N-4-nitrophenylurea
- para-nitrophenylurea
- p-Nitrophenylurea
- Urea, (4-nitrophenyl)-
- Urea, (p-nitrophenyl)-
- 1-(p-Nitrophenyl)urea
- NSC 227938
- 1-(4-Nitrophenyl)urea
- DY0F0348GL
- (4-Nitrophenyl)urea [MI]
- Urea, N-(4-nitrophenyl)-
- Nitrophenylharnstoffe
- amino-N-(4-nitrophenyl)amide
- LXXTVGKSGJADFU-UHFFFAOYSA-N
- NSC227938
- NE48883
- NCGC00320401-0
- AKOS001355782
- NCGC00320401-01
- CS-0244226
- MFCD09040599
- EN300-27378
- Z166687092
- Q27276664
- ent-61327
- T72612
- DTXSID40310514
- 556-10-5
- DB-316712
- AB01315532-02
- UNII-DY0F0348GL
- N0980
- SCHEMBL1102071
- AS-56901
- NSC-227938
-
- MDL: MFCD09040599
- Inchi: 1S/C7H7N3O3/c8-7(11)9-5-1-3-6(4-2-5)10(12)13/h1-4H,(H3,8,9,11)
- InChI Key: LXXTVGKSGJADFU-UHFFFAOYSA-N
- SMILES: [O-][N+](C1C=CC(=CC=1)NC(N)=O)=O
Computed Properties
- Exact Mass: 181.04881
- Monoisotopic Mass: 181.049
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 206
- 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: 1.1
- Topological Polar Surface Area: 101
Experimental Properties
- Density: 1.490
- Melting Point: 217°C(lit.)
- Boiling Point: 314.24°C (rough estimate)
- Flash Point: 160.2°C
- Refractive Index: 1.5860 (estimate)
- PSA: 98.26
- LogP: 2.38190
- Merck: 6626
- λmax: 327(EtOH)(lit.)
(4-Nitrophenyl)urea Security Information
-
Symbol:
- Prompt:warning
- Hazard Statement: H315-H319
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
(4-Nitrophenyl)urea Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | N497235-100mg |
(4-Nitrophenyl)urea |
556-10-5 | 100mg |
45.00 | 2021-07-23 | ||
| TRC | N497235-500mg |
(4-Nitrophenyl)urea |
556-10-5 | 500mg |
$161.00 | 2023-05-17 | ||
| TRC | N497235-1g |
(4-Nitrophenyl)urea |
556-10-5 | 1g |
$ 235.00 | 2022-06-03 | ||
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | N0980-1G |
(4-Nitrophenyl)urea |
556-10-5 | >98.0%(HPLC)(N) | 1g |
¥330.00 | 2023-09-07 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | N0980-5G |
(4-Nitrophenyl)urea |
556-10-5 | >98.0%(HPLC)(N) | 5g |
¥1035.00 | 2023-09-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | N0980-5g |
(4-Nitrophenyl)urea |
556-10-5 | 98.0%(LC&N) | 5g |
¥1290.0 | 2022-06-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | N0980-1g |
(4-Nitrophenyl)urea |
556-10-5 | 98.0%(LC&N) | 1g |
¥330.0 | 2022-06-10 | |
| abcr | AB474629-1 g |
(4-Nitrophenyl)urea, 98%; . |
556-10-5 | 98% | 1g |
€203.60 | 2023-07-18 | |
| abcr | AB474629-5 g |
(4-Nitrophenyl)urea, 98%; . |
556-10-5 | 98% | 5g |
€726.10 | 2023-07-18 | |
| TRC | N497235-2.5g |
(4-Nitrophenyl)urea |
556-10-5 | 2.5g |
$517.00 | 2023-05-17 |
(4-Nitrophenyl)urea Suppliers
(4-Nitrophenyl)urea Related Literature
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Ni-Na Sun,Fengli Qu,Xiaobing Zhang,Shufang Zhang,Jinmao You Analyst, 2015,140, 1827-1831
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
Additional information on (4-Nitrophenyl)urea
Introduction to (4-Nitrophenyl)Urea (CAS No. 556-10-5)
(4-Nitrophenyl)urea, also known as CAS No. 556-10-5, is a chemical compound that has garnered significant attention in the fields of organic chemistry and materials science. This compound is characterized by its unique structure, which combines a urea group with a 4-nitrophenyl substituent. The molecular formula of (4-Nitrophenyl)urea is C7H6N4O3, and its molecular weight is approximately 186.13 g/mol.
The synthesis of (4-Nitrophenyl)urea involves the reaction of 4-nitroaniline with cyanogen chloride in the presence of a base, followed by hydrolysis to yield the urea derivative. This compound is often used as an intermediate in the synthesis of more complex molecules, particularly in the pharmaceutical and agrochemical industries.
Recent studies have highlighted the potential of (4-Nitrophenyl)urea in various applications, including its use as a building block for advanced materials. Researchers have explored its ability to form self-assembled monolayers (SAMs) on surfaces, which can be utilized in the development of sensors and electronic devices. The strong intermolecular hydrogen bonding capability of this compound contributes to its stability in such applications.
In addition to its role in materials science, (4-Nitrophenyl)urea has shown promise in drug discovery efforts. Its structural similarity to certain bioactive compounds makes it a valuable tool for studying molecular interactions and designing new therapeutic agents. For instance, recent investigations have focused on its potential as an inhibitor of specific enzymes involved in metabolic pathways.
The environmental impact of (4-Nitrophenyl)urea has also been a topic of interest. Studies have examined its biodegradation under various conditions, with findings suggesting that it can undergo microbial degradation under aerobic conditions. This information is crucial for assessing its safety and sustainability in industrial applications.
In terms of physical properties, (4-Nitrophenyl)urea is typically a crystalline solid with a melting point around 220°C. It is sparingly soluble in water but exhibits higher solubility in organic solvents such as ethanol and acetone. These properties make it suitable for use in various chemical reactions and formulations.
The demand for (4-Nitrophenyl)urea has been growing due to its versatility and applicability across multiple industries. As research continues to uncover new potential uses for this compound, it is expected to play an increasingly important role in both academic and industrial settings.
In conclusion, (4-Nitrophenyl)urea (CAS No. 556-10-5) is a multifaceted chemical compound with a wide range of applications. Its unique structure and properties make it a valuable asset in the development of new materials, drugs, and technologies. As scientific advancements continue to expand our understanding of this compound, its significance in various fields will undoubtedly grow.
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