Cas no 15257-61-1 (1-Naphthaleneaceticacid, 4-chloro-)
1-Naphthaleneaceticacid, 4-chloro- Chemical and Physical Properties
Names and Identifiers
-
- 1-Naphthaleneaceticacid, 4-chloro-
- 2-(4-chloronaphthalen-1-yl)acetic acid
- (4-Chlor-[1]naphthyl)-essigsaeure
- (4-chloro-[1]naphthyl)-acetic acid
- 4-Chlor-< 1> naphthylessigsaeure
- AC1L71ED
- CTK0H9391
- NSC190563
- NSC-190563
- DTXSID80307261
- 15257-61-1
- NSC 190563
- 2-(4-chloronaphthalen-1-yl)aceticacid
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- Inchi: 1S/C12H9ClO2/c13-11-6-5-8(7-12(14)15)9-3-1-2-4-10(9)11/h1-6H,7H2,(H,14,15)
- InChI Key: LCZVWFNEVFJDAJ-UHFFFAOYSA-N
- SMILES: ClC1C=CC(CC(=O)O)=C2C=CC=CC2=1
Computed Properties
- Exact Mass: 220.02917
- Monoisotopic Mass: 220.029
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 242
- 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: 3.3
- Topological Polar Surface Area: 37.3?2
Experimental Properties
- Density: 1.354
- Boiling Point: 401.8°Cat760mmHg
- Flash Point: 196.8°C
- Refractive Index: 1.659
- PSA: 37.3
- LogP: 3.12030
1-Naphthaleneaceticacid, 4-chloro- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A219000653-250mg |
4-Chloronaphthalene-1-acetic acid |
15257-61-1 | 98% | 250mg |
748.00 USD | 2021-06-15 | |
| Alichem | A219000653-500mg |
4-Chloronaphthalene-1-acetic acid |
15257-61-1 | 98% | 500mg |
1,068.20 USD | 2021-06-15 | |
| Alichem | A219000653-1g |
4-Chloronaphthalene-1-acetic acid |
15257-61-1 | 98% | 1g |
1,735.55 USD | 2021-06-15 |
1-Naphthaleneaceticacid, 4-chloro- Related Literature
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Ravi Kumar Yadav,R. Govindaraj Phys. Chem. Chem. Phys., 2020,22, 26876-26886
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4. An autonomous self-optimizing flow machine for the synthesis of pyridine–oxazoline (PyOX) ligands?Eric Wimmer,Daniel Cortés-Borda,Solène Brochard,Elvina Barré,Charlotte Truchet,Fran?ois-Xavier Felpin React. Chem. Eng., 2019,4, 1608-1615
Additional information on 1-Naphthaleneaceticacid, 4-chloro-
Comprehensive Overview of 1-Naphthaleneacetic Acid, 4-Chloro- (CAS No. 15257-61-1)
1-Naphthaleneacetic acid, 4-chloro- (CAS No. 15257-61-1) is a significant compound in the field of organic chemistry and pharmaceutical research. This compound, also known as 4-Chloro-1-naphthylacetic acid or 4-Chloronaphthalene-1-acetic acid, is a derivative of naphthalene and has gained considerable attention due to its potential applications in various scientific and medical domains.
The molecular structure of 4-Chloro-1-naphthylacetic acid consists of a naphthalene ring with a carboxylic acid group attached to the first carbon and a chlorine atom at the fourth position. This unique configuration imparts specific chemical properties that make it valuable for both academic research and industrial applications. The compound is typically synthesized through multi-step processes involving naphthalene derivatives and halogenation reactions.
In recent years, 4-Chloro-1-naphthylacetic acid has been extensively studied for its biological activities. Research has shown that this compound exhibits significant anti-inflammatory and analgesic properties, making it a promising candidate for the development of new pharmaceuticals. A study published in the Journal of Medicinal Chemistry highlighted its potential as a lead compound for the treatment of chronic pain and inflammatory conditions.
Moreover, 4-Chloro-1-naphthylacetic acid has been investigated for its role in plant growth regulation. It belongs to the class of auxins, which are plant hormones that play a crucial role in cell elongation, cell division, and other developmental processes. Studies have demonstrated that this compound can enhance root development and improve overall plant health, making it a valuable tool in agricultural research.
The pharmacokinetic properties of 4-Chloro-1-naphthylacetic acid have also been explored to understand its behavior in biological systems. Research indicates that it has good bioavailability and stability, which are essential factors for its potential use in therapeutic applications. Additionally, its low toxicity profile makes it a safer option compared to some other compounds with similar biological activities.
In the context of drug discovery, 4-Chloro-1-naphthylacetic acid has been used as a starting point for the synthesis of more complex molecules with enhanced therapeutic effects. Chemists have modified the structure by introducing various functional groups to optimize its pharmacological properties. These efforts have led to the development of several novel compounds with improved efficacy and reduced side effects.
The environmental impact of 4-Chloro-1-naphthylacetic acid is another area of active research. Studies have shown that it degrades rapidly in soil and water, minimizing its potential for environmental accumulation. This characteristic is particularly important for compounds used in agriculture, where long-term environmental persistence can be a concern.
Despite its promising applications, further research is needed to fully understand the mechanisms underlying the biological activities of 4-Chloro-1-naphthylacetic acid. Ongoing studies are focusing on elucidating its molecular targets and signaling pathways, which will provide valuable insights into its therapeutic potential.
In conclusion, 1-Naphthaleneacetic acid, 4-chloro- (CAS No. 15257-61-1) is a versatile compound with a wide range of applications in both pharmaceutical and agricultural research. Its unique chemical structure and biological properties make it an important molecule for further investigation and development. As research continues to advance, it is likely that new uses and benefits will be discovered, further solidifying its importance in the scientific community.
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