Cas no 77858-21-0 (Velaresol)
Velaresol Chemical and Physical Properties
Names and Identifiers
-
- Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-
- 5-(2-Formyl-3-hydroxyphenoxy)pentanoic acid
- 5-(2-formyl-3-hydroxyphenoxy)valeric acid
- 12C
- 12C79
- 2-4'-carboxybutoxy-6-hydroxybenzaldehyde
- BW 12C
- BW-12C
- EINECS 278-778-8
- Velaresol
- UNII-9EQV0XQ79B
- HY-106509
- DTXSID30228472
- 12C79; BW 12C; BW 12C79
- NS00037956
- 5-(2-Formyl-3-Hydroxy-Phenoxy)Pentanoic Acid
- BW12C79
- CS-0025953
- NSUDGNLOXMLAEB-UHFFFAOYSA-N
- VELARESOL [INN]
- 9EQV0XQ79B
- AKOS032960434
- Pentanoic acid, 5-(2-formyl-3-hydroxyphenoxy)-
- 77858-21-0
- BW 12C79
- VELARESOL [MART.]
- SCHEMBL61907
- N16837
- CHEMBL2107643
- BW12C
- BCP20750
- Velaresol [INN:BAN]
- BW-12C79
- Q27272458
- VELARESOL (MART.)
- velaresolum
- DTXCID50150963
- Velaresol?
- DA-68551
- GLXC-10507
-
- MDL: MFCD00867971
- Inchi: 1S/C12H14O5/c13-8-9-10(14)4-3-5-11(9)17-7-2-1-6-12(15)16/h3-5,8,14H,1-2,6-7H2,(H,15,16)
- InChI Key: NSUDGNLOXMLAEB-UHFFFAOYSA-N
- SMILES: O(C1C=CC=C(C=1C=O)O)CCCCC(=O)O
Computed Properties
- Exact Mass: 238.084
- Monoisotopic Mass: 238.084
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 17
- Rotatable Bond Count: 7
- Complexity: 253
- 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
- Topological Polar Surface Area: 83.8A^2
- XLogP3: 1.8
Experimental Properties
- Color/Form: Yellow solid powder
- Density: 1.293
- Boiling Point: 452.3°C at 760 mmHg
- Flash Point: 176.1°C
- Refractive Index: 1.584
Velaresol Security Information
- Signal Word:Warning
- Storage Condition:Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).
Velaresol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | V872125-1mg |
velaresol |
77858-21-0 | 98% | 1mg |
¥415.00 | 2022-01-13 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | V872125-5mg |
velaresol |
77858-21-0 | 98% | 5mg |
¥1,871.00 | 2022-01-13 | |
| eNovation Chemicals LLC | Y0975536-1g |
velaresol |
77858-21-0 | 98% | 1g |
$2580 | 2024-08-03 | |
| DC Chemicals | DC10682-100 mg |
Velaresol |
77858-21-0 | >98% | 100mg |
$450.0 | 2022-02-28 | |
| DC Chemicals | DC10682-250 mg |
Velaresol |
77858-21-0 | >98% | 250mg |
$900.0 | 2022-02-28 | |
| DC Chemicals | DC10682-1 g |
Velaresol |
77858-21-0 | >98% | 1g |
$1800.0 | 2022-02-28 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1097014-1mg |
Velaresol |
77858-21-0 | 98% | 1mg |
¥539 | 2023-04-13 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1097014-5mg |
Velaresol |
77858-21-0 | 98% | 5mg |
¥975.00 | 2024-07-28 | |
| MedChemExpress | HY-106509-5mg |
Velaresol |
77858-21-0 | 99.59% | 5mg |
¥585 | 2025-04-16 | |
| MedChemExpress | HY-106509-10mg |
Velaresol |
77858-21-0 | 99.59% | 10mg |
¥990 | 2025-04-16 |
Velaresol Suppliers
Velaresol Related Literature
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Jason Wan Lab Chip, 2020,20, 4528-4538
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622
Additional information on Velaresol
Introduction to Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)- and its Significance in Modern Chemical Research
Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, a compound with the CAS number 77858-21-0, represents a fascinating molecule in the realm of organic chemistry and pharmaceutical research. This compound, characterized by its intricate structure, has garnered significant attention due to its potential applications in various chemical and biological processes. The unique combination of functional groups, including the formyl and hydroxy moieties, makes it a versatile intermediate for synthesizing more complex molecules.
The molecular structure of Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, consists of a pentanoic acid backbone linked to a phenolic ring that bears both a formyl group and a hydroxyl group. This arrangement not only contributes to its reactivity but also opens up numerous possibilities for further functionalization. The presence of these reactive sites allows for the exploration of diverse chemical transformations, making it a valuable building block in synthetic chemistry.
In recent years, there has been growing interest in the development of novel compounds that can serve as scaffolds for drug discovery. Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, with its dual functionality, has emerged as a promising candidate in this context. The formyl group can participate in condensation reactions to form Schiff bases, while the hydroxyl group can engage in etherification or esterification reactions. These properties make it an attractive molecule for designing new therapeutic agents.
One of the most compelling aspects of Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, is its potential role in medicinal chemistry. Researchers have been exploring its derivatives as candidates for treating various diseases. For instance, studies have shown that compounds derived from this molecule exhibit antimicrobial and anti-inflammatory properties. The ability to modify its structure allows chemists to fine-tune its biological activity, making it possible to develop drugs with enhanced efficacy and reduced side effects.
The synthesis of Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, involves several key steps that highlight the ingenuity of modern synthetic methodologies. The process typically begins with the reaction of 2-formylphenol with pentanoic acid under controlled conditions. This reaction is facilitated by the presence of suitable catalysts that promote the formation of an ester linkage between the two components. Subsequent functionalization steps can then be carried out to introduce additional modifications.
The role of computational chemistry in understanding the behavior of Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)--, cannot be overstated. Advanced computational techniques have enabled researchers to predict the reactivity and stability of this compound with high accuracy. These predictions are crucial for designing efficient synthetic routes and for understanding the mechanisms underlying its biological activity. By leveraging computational methods, scientists can accelerate the discovery process and reduce experimental costs.
In conclusion, Pentanoic acid,5-(2-formyl-3-hydroxyphenoxy)-, is a multifaceted compound with significant potential in both chemical synthesis and pharmaceutical research. Its unique structural features and reactivity make it an invaluable tool for developing new drugs and materials. As research in this field continues to advance, it is likely that we will uncover even more applications for this remarkable molecule.
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