Cas no 10338-69-9 (4-Phenyl-1,2,3,6-tetrahydropyridine)
4-Phenyl-1,2,3,6-tetrahydropyridine Chemical and Physical Properties
Names and Identifiers
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- 4-Phenyl-1,2,3,6-tetrahydropyridine
- 1,2,3,6-tetrahydro-4-phenylpyridine
- 4-Phenyl-1,2,3,6-tetrahydro-pyridine
- 4-Phenyl-1,2,3,6-tetrahydro-pyridin
- 4-phenyl-1,2,5,6-tetrahydropyridine
- Pyridine,1,2,3,6-tetrahydro-4-phenyl
- 4-Phenyl-1,2,3,6-tetrahydropyridine, AldrichCPR
- Pyridine,2,3,6-tetrahydro-4-phenyl-
- PD182313
- Pyridine, 1,2,3,6-tetrahydro-4-phenyl-
- A13901
- 4-Phenyl-1,2,3,6-tetra-Hydropyridine
- SCHEMBL415545
- NSC-54451
- AKOS005466795
- Z1742056028
- CS-0171304
- 4- phenyl-1,2,3,6-tetrahydropyridine
- NSC54451
- CHEMBL6224
- NSC 54451
- Oprea1_874761
- EN300-35076
- FT-0619379
- 10338-69-9
- AS-35405
- BDBM50036718
- MFCD00023118
- NCGC00246414-01
- 4-(phenyl)-1,2,5,6-tetrahydropyridine
- 4-Phenyl-1,3,6-tetrahydropyridine
- 1,2,3,6-tetrahydro-4-phenyl-pyridine
- DTXSID2065040
- BBL027886
- DB-040447
- STK535809
-
- MDL: MFCD00023118
- Inchi: 1S/C11H13N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-6,12H,7-9H2
- InChI Key: OMPXTQYWYRWWPH-UHFFFAOYSA-N
- SMILES: N1CC=C(C2C=CC=CC=2)CC1
Computed Properties
- Exact Mass: 195.08100
- Monoisotopic Mass: 195.081477
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 12
- Rotatable Bond Count: 1
- Complexity: 166
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 12
- XLogP3: 2
Experimental Properties
- Color/Form: Yellow to Brown Liquid
- Density: 1.008
- Boiling Point: 267.9 oC
- Flash Point: 119.9 oC
- PSA: 12.03000
- LogP: 3.19410
4-Phenyl-1,2,3,6-tetrahydropyridine Security Information
- Signal Word:Warning
- Hazard Statement: H302;H319;H411
- Warning Statement: P273;P305+P351+P338
- Hazard Category Code: 22-36-51
- Safety Instruction: 26
-
Hazardous Material Identification:
- Storage Condition:2-8 °C
4-Phenyl-1,2,3,6-tetrahydropyridine Customs Data
- HS CODE:2933399090
- Customs Data:
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
4-Phenyl-1,2,3,6-tetrahydropyridine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P228985-500mg |
4-Phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 500mg |
$ 480.00 | 2022-06-03 | ||
| TRC | P228985-1000mg |
4-Phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 1g |
$ 800.00 | 2022-06-03 | ||
| TRC | P228985-2000mg |
4-Phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 2g |
$ 1280.00 | 2022-06-03 | ||
| Fluorochem | 040214-5g |
4-Phenyl-1,2,3,6-tetrahydro-pyridine |
10338-69-9 | 98% | 5g |
£52.00 | 2022-03-01 | |
| Fluorochem | 040214-25g |
4-Phenyl-1,2,3,6-tetrahydro-pyridine |
10338-69-9 | 98% | 25g |
£182.00 | 2022-03-01 | |
| Chemenu | CM133680-1g |
4-phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 95% | 1g |
$230 | 2021-08-05 | |
| Chemenu | CM133680-5g |
4-phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 95% | 5g |
$608 | 2021-08-05 | |
| eNovation Chemicals LLC | D780703-1g |
4-Phenyl-1,2,3,6-tetrahydro pyridine |
10338-69-9 | 95% | 1g |
$295 | 2024-08-03 | |
| Chemenu | CM133680-1g |
4-phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 95% | 1g |
$230 | 2023-02-19 | |
| Chemenu | CM133680-5g |
4-phenyl-1,2,3,6-tetrahydropyridine |
10338-69-9 | 95% | 5g |
$608 | 2023-02-19 |
4-Phenyl-1,2,3,6-tetrahydropyridine Suppliers
4-Phenyl-1,2,3,6-tetrahydropyridine Related Literature
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
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Kaiyuan Huang,Wangkang Qiu,Meilian Ou,Xiaorui Liu,Zenan Liao,Sheng Chu RSC Adv., 2020,10, 18824-18829
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
Additional information on 4-Phenyl-1,2,3,6-tetrahydropyridine
Exploring the Versatile Applications and Properties of 4-Phenyl-1,2,3,6-tetrahydropyridine (CAS No. 10338-69-9)
4-Phenyl-1,2,3,6-tetrahydropyridine (CAS No. 10338-69-9) is a fascinating organic compound that has garnered significant attention in both academic and industrial research. This compound, often referred to as 4-Phenyl-THP, belongs to the tetrahydropyridine family, which is known for its diverse applications in medicinal chemistry, material science, and synthetic organic chemistry. The presence of a phenyl group at the 4-position of the tetrahydropyridine ring imparts unique chemical properties, making it a valuable intermediate in the synthesis of more complex molecules.
The molecular structure of 4-Phenyl-1,2,3,6-tetrahydropyridine features a partially saturated pyridine ring, which contributes to its reactivity and versatility. Researchers have explored its potential as a building block for pharmaceuticals, particularly in the development of central nervous system (CNS) targeting agents. The compound's ability to cross the blood-brain barrier has made it a subject of interest in neurodegenerative disease research, aligning with current trends in neuroprotective drug development and brain health supplements.
In recent years, the demand for 4-Phenyl-THP derivatives has increased due to their potential applications in cognitive enhancement and memory improvement formulations. This aligns with the growing consumer interest in nootropics and brain-boosting compounds. The compound's structural similarity to certain alkaloids found in nature has also sparked interest in its potential as a natural product mimic, a hot topic in green chemistry and sustainable drug discovery.
From a synthetic chemistry perspective, 4-Phenyl-1,2,3,6-tetrahydropyridine serves as an excellent scaffold for heterocyclic compound synthesis. Its reactivity allows for various functionalization strategies, making it a favorite among medicinal chemists working on structure-activity relationship studies. The compound's stability under various conditions also makes it suitable for high-throughput screening applications in drug discovery pipelines.
The pharmaceutical industry has shown particular interest in 4-Phenyl-THP based compounds for their potential as dopamine receptor modulators. This application ties into current research trends focusing on neurotransmitter regulation and mood disorder treatments. The compound's structural features make it a promising candidate for developing novel therapeutics targeting conditions like Parkinson's disease and depression, without the side effects associated with traditional treatments.
Material scientists have also explored applications of 4-Phenyl-1,2,3,6-tetrahydropyridine in organic electronics and conductive polymers. The aromatic system combined with the nitrogen heteroatom creates interesting electronic properties that could be valuable in developing new organic semiconductors. This aligns perfectly with the current push for more efficient and sustainable electronic materials.
In the field of catalysis, derivatives of 4-Phenyl-THP have shown promise as ligands for transition metal catalysts. This application is particularly relevant given the growing emphasis on green chemistry and sustainable synthesis methods. Researchers are investigating how these compounds can facilitate more efficient chemical transformations with lower environmental impact.
The compound's stability and relatively simple synthesis make it an attractive target for process chemistry optimization. Many pharmaceutical companies are focusing on developing cost-effective and scalable synthetic routes to 4-Phenyl-1,2,3,6-tetrahydropyridine and its derivatives, addressing the industry's need for efficient manufacturing processes.
Analytical chemists have developed various methods for characterizing 4-Phenyl-THP, including advanced techniques like NMR spectroscopy and mass spectrometry. These methods are crucial for quality control in both research and industrial settings, especially given the compound's increasing importance in medicinal chemistry applications.
Looking to the future, 4-Phenyl-1,2,3,6-tetrahydropyridine continues to be a compound of significant interest across multiple scientific disciplines. Its versatility as a synthetic intermediate, combined with its potential biological activities, ensures it will remain relevant in drug discovery, material science, and catalysis research for years to come. As research into its properties and applications continues to expand, we can expect to see novel uses emerge in fields ranging from agricultural chemistry to flavor and fragrance development.
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