Cas no 129786-94-3 ((2-benzylphenyl)hydrazine)
(2-benzylphenyl)hydrazine Chemical and Physical Properties
Names and Identifiers
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- Hydrazine, [2-(phenylmethyl)phenyl]- (9CI)
- hydrazine, [2-(phenylmethyl)phenyl]-
- (2-benzylphenyl)hydrazine
- [2-(Phenylmethyl)phenyl]hydrazine
- AKOS011538605
- a-Benzylphenylhydrazin
- DTXSID60396976
- EN300-266167
- SCHEMBL2137543
- 129786-94-3
-
- MDL: MFCD02663163
- Inchi: 1S/C13H14N2/c14-15-13-9-5-4-8-12(13)10-11-6-2-1-3-7-11/h1-9,15H,10,14H2
- InChI Key: HWRVFQYVRDGGBP-UHFFFAOYSA-N
- SMILES: N(C1C=CC=CC=1CC1C=CC=CC=1)N
Computed Properties
- Exact Mass: 198.11582
- Monoisotopic Mass: 198.115698455g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 3
- Complexity: 175
- 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: 3.1
- Topological Polar Surface Area: 38?2
Experimental Properties
- Density: 1.129
- Melting Point: 148-149 oC
- PSA: 38.05
(2-benzylphenyl)hydrazine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
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| Enamine | EN300-266167-0.05g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 0.05g |
$419.0 | 2023-09-12 | ||
| Enamine | EN300-266167-0.1g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 0.1g |
$439.0 | 2023-09-12 | ||
| Enamine | EN300-266167-0.25g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 0.25g |
$459.0 | 2023-09-12 | ||
| Enamine | EN300-266167-0.5g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 0.5g |
$479.0 | 2023-09-12 | ||
| Enamine | EN300-266167-1.0g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 1g |
$0.0 | 2023-06-07 | ||
| Enamine | EN300-266167-2.5g |
(2-benzylphenyl)hydrazine |
129786-94-3 | 2.5g |
$978.0 | 2023-09-12 | ||
| Enamine | EN300-266167-5.0g |
(2-benzylphenyl)hydrazine |
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$1448.0 | 2023-03-01 | ||
| Enamine | EN300-266167-10.0g |
(2-benzylphenyl)hydrazine |
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$2146.0 | 2023-03-01 | ||
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1579401-50mg |
(2-Benzylphenyl)hydrazine |
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| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1579401-100mg |
(2-Benzylphenyl)hydrazine |
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¥11524.00 | 2024-08-09 |
(2-benzylphenyl)hydrazine Suppliers
(2-benzylphenyl)hydrazine Related Literature
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Byungho Lim,Jaewon Jin,Jin Yoo,Seung Yong Han,Kyeongyeol Kim,Sungah Kang,Nojin Park,Sang Moon Lee,Hae Jin Kim,Seung Uk Son Chem. Commun., 2014,50, 7723-7726
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Jason Wan Lab Chip, 2020,20, 4528-4538
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Erika A. Cobar,Paul R. Horn,Robert G. Bergman,Martin Head-Gordon Phys. Chem. Chem. Phys., 2012,14, 15328-15339
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Qiaoe Wang,Meiling Lian,Xiaowen Zhu,Xu Chen RSC Adv., 2021,11, 192-197
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Chao-Han Cheng,Wen-Zhen Wang,Shie-Ming Peng,I-Chia Chen Phys. Chem. Chem. Phys., 2017,19, 25471-25477
Additional information on (2-benzylphenyl)hydrazine
Introduction to (2-Benzylphenyl)Hydrazine (CAS No. 129786-94-3)
Hydrazine derivatives have long been a subject of interest in organic chemistry due to their versatile applications in pharmaceuticals, agrochemicals, and materials science. Among these, (2-benzylphenyl)hydrazine (CAS No. 129786-94-3) stands out as a compound with unique structural and functional properties. This article delves into the latest research findings, chemical characteristics, and potential applications of this compound, providing a comprehensive overview for researchers and industry professionals.
The chemical structure of (2-benzylphenyl)hydrazine consists of a hydrazine group (-NHNH2) attached to a benzene ring substituted with a benzyl group at the 2-position. This arrangement imparts the molecule with aromatic stability and enhances its reactivity in various chemical reactions. Recent studies have highlighted the importance of such structural features in determining the compound's pharmacokinetic properties and its potential as a building block in drug design.
From a synthetic perspective, (2-benzylphenyl)hydrazine can be synthesized through several methods, including the condensation of hydrazine with substituted aromatic aldehydes or ketones. Researchers have explored green chemistry approaches to optimize these reactions, reducing environmental impact while maintaining high yields. For instance, microwave-assisted synthesis has been shown to significantly accelerate the formation of this compound, making it more feasible for large-scale production.
The application of (2-benzylphenyl)hydrazine extends beyond traditional organic synthesis. Recent advancements have demonstrated its utility in the development of novel materials, such as coordination polymers and metal-organic frameworks (MOFs). These materials exhibit exceptional porosity and selectivity, making them promising candidates for gas storage and catalytic applications. Additionally, studies on the electrochemical properties of (2-benzylphenyl)hydrazine derivatives have revealed their potential as active components in batteries and sensors.
In the pharmaceutical sector, (2-benzylphenyl)hydrazine has gained attention as a lead compound for anti-inflammatory and anticancer drug development. Preclinical studies have shown that certain derivatives exhibit potent inhibitory effects on inflammatory pathways and tumor growth in vitro. Furthermore, ongoing research is exploring its role as a scaffold for designing enzyme inhibitors, leveraging its ability to form hydrogen bonds with biomolecular targets.
From an environmental standpoint, understanding the fate and toxicity of (2-benzylphenyl)hydrazine is crucial for its safe handling and disposal. Recent toxicological studies have provided insights into its acute and chronic effects on aquatic organisms, guiding regulatory frameworks for industrial use. Moreover, biodegradation pathways have been identified, offering strategies to minimize its environmental footprint.
In conclusion, (2-benzylphenyl)hydrazine (CAS No. 129786-94-3) is a multifaceted compound with significant potential across diverse fields. By integrating cutting-edge research findings with practical applications, this article underscores its importance as a valuable tool in modern chemistry. As advancements continue to unfold, further exploration of its properties will undoubtedly unlock new opportunities for innovation and sustainable development.
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