Cas no 143667-36-1 (4-Phenoxybenzohydrazide)
4-Phenoxybenzohydrazide Chemical and Physical Properties
Names and Identifiers
-
- Benzoic acid,4-phenoxy-, hydrazide
- 4-PHENOXYBENZHYDRAZIDE
- 4-phenoxybenzohydrazide
- ETHYL3-AMINO-4-(ISOPROPYLSULFONYL)-5-(METHYLTHIO)THIOPHENE-2-CARBOXYLATE
- DTXSID70375116
- 143667-36-1
- BS-42396
- SCHEMBL2835202
- 1-phenoxybenzene-4-carbohydrazide
- CS-0360495
- FT-0682117
- AKOS015855150
- SB86449
- MFCD00153894
- Z58981836
- LRBASDKESQRLCX-UHFFFAOYSA-N
- STK331011
- DB-106955
- 4-Phenoxybenzohydrazide
-
- MDL: MFCD00153894
- Inchi: 1S/C13H12N2O2/c14-15-13(16)10-6-8-12(9-7-10)17-11-4-2-1-3-5-11/h1-9H,14H2,(H,15,16)
- InChI Key: LRBASDKESQRLCX-UHFFFAOYSA-N
- SMILES: O(C1C=CC=CC=1)C1C=CC(C(NN)=O)=CC=1
Computed Properties
- Exact Mass: 228.09000
- Monoisotopic Mass: 228.09
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 17
- Rotatable Bond Count: 4
- Complexity: 244
- 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: 1.7
- Topological Polar Surface Area: 64.4A^2
Experimental Properties
- Density: 1.217
- Melting Point: 125-127°C
- Boiling Point: °Cat760mmHg
- Flash Point: °C
- Refractive Index: 1.612
- PSA: 64.35000
- LogP: 3.17360
4-Phenoxybenzohydrazide Customs Data
- HS CODE:2928000090
- Customs Data:
China Customs Code:
2928000090Overview:
2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%
Declaration elements:
Product Name, component content, use to
Summary:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%
4-Phenoxybenzohydrazide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 018946-1g |
4-Phenoxybenzhydrazide |
143667-36-1 | 1g |
£17.00 | 2022-03-01 | ||
| Fluorochem | 018946-5g |
4-Phenoxybenzhydrazide |
143667-36-1 | 5g |
£71.00 | 2022-03-01 | ||
| Fluorochem | 018946-25g |
4-Phenoxybenzhydrazide |
143667-36-1 | 25g |
£325.00 | 2022-03-01 | ||
| TRC | P318370-50mg |
4-Phenoxybenzohydrazide |
143667-36-1 | 50mg |
$ 50.00 | 2022-06-03 | ||
| TRC | P318370-100mg |
4-Phenoxybenzohydrazide |
143667-36-1 | 100mg |
$ 65.00 | 2022-06-03 | ||
| TRC | P318370-500mg |
4-Phenoxybenzohydrazide |
143667-36-1 | 500mg |
$ 80.00 | 2022-06-03 | ||
| abcr | AB149809-5 g |
4-Phenoxybenzhydrazide; 97% |
143667-36-1 | 5g |
€174.00 | 2023-05-09 | ||
| abcr | AB149809-25 g |
4-Phenoxybenzhydrazide; 97% |
143667-36-1 | 25g |
€537.80 | 2023-05-09 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-280459-5 g |
4-Phenoxybenzhydrazide, |
143667-36-1 | 5g |
¥579.00 | 2023-07-11 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-280459A-25 g |
4-Phenoxybenzhydrazide, |
143667-36-1 | 25g |
¥2,324.00 | 2023-07-11 |
4-Phenoxybenzohydrazide Suppliers
4-Phenoxybenzohydrazide Related Literature
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Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
-
Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
Additional information on 4-Phenoxybenzohydrazide
4-Phenoxybenzohydrazide (CAS No. 143667-36-1): A Comprehensive Overview of Properties and Applications
4-Phenoxybenzohydrazide (CAS No. 143667-36-1) is an organic compound that has garnered significant attention in recent years due to its versatile applications in pharmaceutical research and material science. This hydrazide derivative features a phenoxybenzene core structure, making it a valuable intermediate for synthesizing more complex molecules. With the growing interest in drug discovery and organic synthesis, researchers are increasingly exploring the potential of 4-Phenoxybenzohydrazide in developing novel therapeutic agents and functional materials.
The molecular structure of 4-Phenoxybenzohydrazide consists of a benzohydrazide moiety linked to a phenoxy group, which contributes to its unique chemical properties. This compound is known for its moderate solubility in polar organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), while exhibiting limited solubility in water. Its melting point typically ranges between 150-160°C, and it appears as a white to off-white crystalline powder under standard conditions. These physical characteristics make it suitable for various laboratory and industrial applications.
In the pharmaceutical sector, 4-Phenoxybenzohydrazide has emerged as a promising building block for medicinal chemistry. Recent studies highlight its potential as a precursor for developing antimicrobial agents, particularly in the fight against drug-resistant pathogens—a pressing global health concern. The compound's ability to form stable complexes with metal ions also makes it valuable in designing metal-based therapeutics, which are gaining traction in cancer treatment research. Furthermore, its structural features allow for easy modification, enabling medicinal chemists to create diverse derivatives with tailored biological activities.
The material science field has also benefited from applications of 4-Phenoxybenzohydrazide. Its aromatic structure and functional groups make it an excellent candidate for developing advanced polymers and coordination compounds. Researchers are investigating its use in creating high-performance materials with enhanced thermal stability and mechanical properties, addressing the growing demand for sustainable and durable materials in various industries. Additionally, its potential in corrosion inhibition has sparked interest among scientists working on metal protection technologies.
From a synthetic chemistry perspective, 4-Phenoxybenzohydrazide serves as a versatile intermediate in organic transformations. It participates in various reactions, including condensation, cyclization, and nucleophilic substitution, making it valuable for constructing heterocyclic compounds. The compound's reactivity has been particularly useful in developing fluorescence probes and sensor materials, which are crucial for environmental monitoring and biomedical diagnostics. These applications align with current trends in green chemistry and sustainable technology development.
The market for 4-Phenoxybenzohydrazide has shown steady growth, driven by increasing research activities in pharmaceutical and material science sectors. Suppliers typically offer this compound with high purity grades (≥98%) to meet the stringent requirements of research laboratories and industrial applications. Quality control measures include rigorous HPLC analysis and spectroscopic characterization to ensure batch-to-batch consistency. Proper storage recommendations include keeping the compound in a cool, dry place away from direct sunlight to maintain its stability over extended periods.
Safety considerations for handling 4-Phenoxybenzohydrazide follow standard laboratory protocols for organic compounds. While not classified as highly hazardous, appropriate personal protective equipment (PPE) including gloves and safety glasses is recommended when working with this material. Proper ventilation should be maintained in working areas, and standard procedures for chemical waste disposal should be followed. These precautions align with current laboratory safety standards and responsible research practices emphasized in modern scientific communities.
Recent advancements in synthetic methodologies have improved the production efficiency of 4-Phenoxybenzohydrazide, making it more accessible to researchers worldwide. Novel catalytic systems and green synthesis approaches have reduced reaction times and improved yields while minimizing environmental impact. These developments support the growing demand for this compound in both academic and industrial settings, particularly in regions with strong pharmaceutical and materials research sectors.
Looking ahead, the future prospects for 4-Phenoxybenzohydrazide appear promising. Ongoing research continues to uncover new applications, particularly in bioconjugation chemistry and drug delivery systems. The compound's structural versatility positions it well for innovation in multiple scientific disciplines. As synthetic chemistry techniques advance and interdisciplinary research expands, 4-Phenoxybenzohydrazide is likely to play an increasingly important role in developing next-generation materials and therapeutic agents.
For researchers and industry professionals seeking detailed technical information about 4-Phenoxybenzohydrazide (CAS No. 143667-36-1), comprehensive analytical data including NMR spectra, mass spectrometry results, and chromatographic purity profiles are typically available from reputable chemical suppliers. These resources facilitate proper characterization and application of the compound in various research and development projects, supporting innovation across multiple scientific fields.
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