Cas no 37177-16-5 (Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester)
Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester Chemical and Physical Properties
Names and Identifiers
-
- Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester
- butyl 4-[(4-hexoxyphenyl)methylideneamino]benzoate
- BUTYL P-HEXYLOXYBENZYLIDENE P-AMINOBENZOATE ---LIQUID CRYSTAL---
- butyl 4-[(1E)-2-(4-hexyloxyphenyl)-1-azavinyl]benzoate
- FT-0623317
- 37177-16-5
- BUTYLP-HEXYLOXYBENZYLIDENEP-AMINOBENZOATE
- Butyl 4-[(E)-{[4-(hexyloxy)phenyl]methylidene}amino]benzoate
- AKOS032953556
- (E)-butyl 4-(4-(hexyloxy)benzylideneamino)benzoate
- SCHEMBL12416648
- butyl p-hexyloxybenzylidene p-aminobenzoate
- DTXSID30592347
- MFCD00043674
-
- Inchi: 1S/C24H31NO3/c1-3-5-7-8-18-27-23-15-9-20(10-16-23)19-25-22-13-11-21(12-14-22)24(26)28-17-6-4-2/h9-16,19H,3-8,17-18H2,1-2H3/b25-19+
- InChI Key: MKPUCYFWMJISAK-NCELDCMTSA-N
- SMILES: O(C1C=CC(/C=N/C2C=CC(=CC=2)C(=O)OCCCC)=CC=1)CCCCCC
Computed Properties
- Exact Mass: 381.23000
- Monoisotopic Mass: 381.23039385g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 28
- Rotatable Bond Count: 13
- Complexity: 435
- 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: 6.6
- Topological Polar Surface Area: 47.9?2
Experimental Properties
- PSA: 47.89000
- LogP: 6.35320
Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| 1PlusChem | 1P00C7Y6-1g |
BUTYL P-HEXYLOXYBENZYLIDENE P-AMINOBENZOATE |
37177-16-5 | 1g |
$114.00 | 2024-05-04 | ||
| A2B Chem LLC | AF69374-1g |
BUTYL P-HEXYLOXYBENZYLIDENE P-AMINOBENZOATE |
37177-16-5 | 1g |
$107.00 | 2024-04-20 |
Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester Related Literature
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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2. An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3nanoparticlesAdrian Brandt,Florian Winter,Sebastian Klamor,Frank Berkemeier,Jatinkumar Rana,Rainer P?ttgen,Andrea Balducci J. Mater. Chem. A, 2013,1, 11229-11236
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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Karl Crowley,Eimer O'Malley,Aoife Morrin,Malcolm R. Smyth,Anthony J. Killard Analyst, 2008,133, 391-399
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H. V. Jain,D. Verthelyi,S. L. Beaucage RSC Adv., 2017,7, 42519-42528
Additional information on Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester
Research Brief on Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester (CAS: 37177-16-5)
Recent studies on Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester (CAS: 37177-16-5) have highlighted its potential applications in the field of chemical biology and pharmaceutical sciences. This compound, characterized by its unique molecular structure, has been the subject of investigation due to its promising biological activities and potential therapeutic benefits. The following brief provides an overview of the latest research findings, methodologies, and implications related to this compound.
The primary focus of recent research has been on elucidating the compound's mechanism of action and its interactions with biological targets. Studies utilizing advanced spectroscopic techniques, such as NMR and mass spectrometry, have confirmed the structural integrity and stability of Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester under various physiological conditions. These findings are critical for understanding its pharmacokinetic properties and potential as a drug candidate.
In vitro and in vivo experiments have demonstrated the compound's efficacy in modulating specific biochemical pathways. For instance, research has shown that it exhibits significant inhibitory effects on certain enzymes involved in inflammatory responses, suggesting its potential as an anti-inflammatory agent. Additionally, preliminary data indicate that the compound may possess antimicrobial properties, making it a candidate for further exploration in infectious disease therapeutics.
The synthesis and optimization of Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester have also been a key area of investigation. Recent advancements in synthetic chemistry have enabled the production of this compound with higher yields and purity, which is essential for scaling up potential pharmaceutical applications. Researchers have employed green chemistry principles to minimize environmental impact during synthesis, aligning with the growing demand for sustainable drug development practices.
Despite these promising findings, challenges remain in the development of this compound for clinical use. Issues such as bioavailability, toxicity, and long-term stability need to be addressed through further preclinical studies. Collaborative efforts between academic institutions and pharmaceutical companies are underway to overcome these hurdles and accelerate the translation of research findings into practical applications.
In conclusion, Benzoic acid,4-[[[4-(hexyloxy)phenyl]methylene]amino]-, butyl ester (CAS: 37177-16-5) represents a promising candidate in the realm of chemical biology and drug discovery. Continued research and development efforts are expected to unlock its full potential, paving the way for novel therapeutic interventions. This brief underscores the importance of interdisciplinary collaboration and innovative methodologies in advancing the field of chemical biology and pharmaceutical sciences.
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