Cas no 1771-18-2 (2-Methoxy Phenothiazine)
2-Methoxy Phenothiazine Chemical and Physical Properties
Names and Identifiers
-
- 2-Methoxy-10H-phenothiazine
- Phenothiazine, 2-methoxy-
- 10H-PHENOTHIAZINE, 2-METHOXY-
- Methyl phenothiazin-2-yl ether
- 2-MethoxyPhenthiazine
- MethoxyPhenoThiazine
- 2-Methoxy-phenothiazine
- 2-Methoxyphenothiazine
- 2-Methoxy Phenothiaz
- 10H-PHENOTHIAZINE,2-METHOXY
- 2-Methoxy-phenothiazin
- MagnesiuM hydroxide
- Phenothiazine,2-methoxy
- DLYKFPHPBCTAKD-UHFFFAOYSA-N
- C13H11NOS
- NSC72107
- 2methoxy-phenothiazine
- PubChem10722
- 2-Methoxy Phenothiazine
- TimTec1_000536
- Oprea1_747823
- cid_74490
- 10H-Phenothiazine,2-metho
- NSC 72107
- CHEBI:125620
- DTXSID70170249
- EN300-02378
- SCHEMBL239600
- NS00025837
- EINECS 217-195-5
- AKOS001305620
- HY-W012258
- Levomepromazine Maleate Imp. A (EP); Levomepromazine Imp. A (EP); 2-Methoxyphenothiazine; Levomepromazine Maleate Impurity A; Levomepromazine Impurity A
- CHEMBL64404
- Z87002126
- NSC-72107
- W-107831
- AM10783
- 1771-18-2
- BRD-K70980943-001-01-1
- MFCD00037838
- SR-03000000753-1
- PD055439
- Q27216232
- AC-16556
- BDBM50012881
- CS-W012974
- SY053063
- D91390
- M0822
- AS-59826
- FT-0612858
- HMS1535I08
- ALBB-025822
- DTXSID301295815
- 10H-Phenothiazin-10-yl, 2-methoxy-
- DB-014140
- 63245-41-0
- DTXCID0092740
- STK400090
- 217-195-5
- FM70658
- 2-Methoxy-10H-phenothiazine;Methyl phenothiazin-2-yl ether;NSC 72107
-
- MDL: MFCD00037838
- Inchi: 1S/C13H11NOS/c1-15-9-6-7-13-11(8-9)14-10-4-2-3-5-12(10)16-13/h2-8,14H,1H3
- InChI Key: DLYKFPHPBCTAKD-UHFFFAOYSA-N
- SMILES: S1C2C=CC=CC=2NC2C=C(C=CC1=2)OC
Computed Properties
- Exact Mass: 229.05600
- Monoisotopic Mass: 229.056135
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 16
- Rotatable Bond Count: 1
- Complexity: 248
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 4.1
- Topological Polar Surface Area: 46.6
Experimental Properties
- Color/Form: Yellowish or grayish solid
- Density: 1.2350
- Melting Point: 185-188 oC
- Boiling Point: 408.1 oC at 760 mmHg
- Flash Point: 200.6oC
- Refractive Index: 1.646
- PSA: 46.56000
- LogP: 4.04140
- Solubility: Not determined
2-Methoxy Phenothiazine Security Information
- Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36/37/39
- Risk Phrases:R36/37/38
2-Methoxy Phenothiazine Customs Data
- HS CODE:2934300000
- Customs Data:
China Customs Code:
2934300000Overview:
2934300000. Compounds containing a phenothiazine ring system(Phenothiazine ring system, whether hydrogenated or not,Compounds not further fused ). 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
Summary:
2934300000. other compounds containing in the structure a phenothiazine ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
2-Methoxy Phenothiazine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | M0822-25G |
2-Methoxyphenothiazine |
1771-18-2 | >98.0%(HPLC) | 25g |
¥170.00 | 2024-04-17 | |
| TRC | M265330-1g |
2-Methoxy Phenothiazine |
1771-18-2 | 1g |
$ 87.00 | 2023-09-07 | ||
| TRC | M265330-5g |
2-Methoxy Phenothiazine |
1771-18-2 | 5g |
$119.00 | 2023-05-18 | ||
| TRC | M265330-10g |
2-Methoxy Phenothiazine |
1771-18-2 | 10g |
$187.00 | 2023-05-18 | ||
| TRC | M265330-25g |
2-Methoxy Phenothiazine |
1771-18-2 | 25g |
$447.00 | 2023-05-18 | ||
| Chemenu | CM304366-500g |
2-Methoxy-10H-phenothiazine |
1771-18-2 | 95% | 500g |
$598 | 2021-08-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | M62150-25g |
2-Methoxy-10H-phenothiazine |
1771-18-2 | 25g |
¥948.0 | 2021-09-08 | ||
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | M62150-100g |
2-Methoxy-10H-phenothiazine |
1771-18-2 | 100g |
¥2688.0 | 2021-09-08 | ||
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R028241-100g |
2-Methoxy Phenothiazine |
1771-18-2 | 98% | 100g |
¥583 | 2024-05-25 | |
| SHANG HAI YI EN HUA XUE JI SHU Co., Ltd. | R028241-25g |
2-Methoxy Phenothiazine |
1771-18-2 | 98% | 25g |
¥152 | 2024-05-25 |
2-Methoxy Phenothiazine Suppliers
2-Methoxy Phenothiazine Related Literature
-
Amy C. Dodds,Sabrina Puddu,Andrew Sutherland Org. Biomol. Chem. 2022 20 5602
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Chang Liu,Xiaojie Jiao,Qing Wang,Kun Huang,Song He,Liancheng Zhao,Xianshun Zeng Chem. Commun. 2017 53 10727
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N. P. Buu-Ho?,B. Lobert,G. Saint-Ruf J. Chem. Soc. C 1969 2137
Additional information on 2-Methoxy Phenothiazine
Introduction to 2-Methoxy Phenothiazine (CAS No. 1771-18-2) and Its Emerging Applications in Chemical and Pharmaceutical Research
2-Methoxy Phenothiazine, identified by the Chemical Abstracts Service Number (CAS No.) 1771-18-2, is a heterocyclic organic compound belonging to the phenothiazine class. This compound has garnered significant attention in the fields of medicinal chemistry and chemical biology due to its unique structural properties and versatile pharmacological potential. Phenothiazines, as a class, are well-known for their broad spectrum of biological activities, including antipsychotic, antihistaminic, and antimicrobial effects. The introduction of a methoxy group at the 2-position of the phenothiazine core modifies its electronic and steric characteristics, thereby influencing its interaction with biological targets.
The chemical structure of 2-Methoxy Phenothiazine consists of a phenothiazine ring system substituted with a methoxy group at the 2-position and a hydrogen atom at the 10-position. This configuration imparts distinct electronic properties, making it a valuable scaffold for drug design and development. The phenothiazine core is characterized by a tricyclic structure comprising a benzene ring fused to a thiophene ring, which is further connected to a pyridine-like nitrogen-containing ring. The presence of nitrogen atoms in the ring system allows for various hydrogen bonding interactions, enhancing its binding affinity to biological macromolecules.
In recent years, 2-Methoxy Phenothiazine has been extensively studied for its potential applications in chemical biology and pharmaceutical research. One of the most notable areas of interest is its role as an intermediate in the synthesis of more complex pharmacophores. Researchers have leveraged its structural framework to develop novel compounds with enhanced therapeutic profiles. For instance, modifications at the 5- and 10-positions of the phenothiazine ring have led to the discovery of new antimicrobial agents that exhibit improved efficacy against resistant bacterial strains.
Moreover, 2-Methoxy Phenothiazine has been explored as a modulator of enzyme activity and receptor binding. Its ability to interact with various biological targets makes it a promising candidate for developing drugs targeting neurological disorders, such as schizophrenia and Parkinson's disease. Recent studies have demonstrated that derivatives of 2-Methoxy Phenothiazine can modulate neurotransmitter receptors, including dopamine receptors, which are implicated in these conditions. The methoxy group at the 2-position plays a crucial role in fine-tuning the pharmacokinetic properties of these derivatives, enhancing their bioavailability and reducing side effects.
The synthesis of 2-Methoxy Phenothiazine typically involves multi-step organic reactions starting from commercially available precursors. Common synthetic routes include Friedel-Crafts acylation followed by nucleophilic substitution or cyclization reactions. Advances in synthetic methodologies have enabled the efficient preparation of this compound in high yields, facilitating further research into its pharmacological properties. The availability of high-purity 2-Methoxy Phenothiazine (CAS No. 1771-18-2) from reputable suppliers has been instrumental in conducting detailed structural-activity relationship (SAR) studies.
From a computational chemistry perspective, 2-Methoxy Phenothiazine has been subjected to extensive molecular modeling studies to elucidate its interactions with biological targets. Quantum mechanical calculations have provided insights into the electronic structure and reactivity of this compound, aiding in the rational design of more potent derivatives. These computational approaches have also helped in predicting drug-like properties such as solubility, permeability, and metabolic stability, which are critical for optimizing drug candidates.
The pharmacological profile of 2-Methoxy Phenothiazine extends beyond traditional applications in psychiatry and neurology. Emerging research suggests its potential in combating infectious diseases caused by resistant pathogens. Studies have shown that certain derivatives exhibit broad-spectrum antimicrobial activity by interfering with bacterial cell wall synthesis or DNA replication. This finding underscores the versatility of phenothiazine derivatives as therapeutic agents against emerging infectious threats.
In addition to its medicinal applications, 2-Methoxy Phenothiazine has found utility in materials science and chemical sensors. Its ability to form stable complexes with metal ions makes it suitable for designing luminescent probes for biochemical assays. These probes can be used to detect trace amounts of metal ions in environmental samples or biological fluids, offering valuable tools for analytical chemistry research.
The future directions of research on 2-Methoxy Phenothiazine (CAS No. 1771-18-2) are likely to focus on expanding its therapeutic applications through structural optimization and interdisciplinary collaborations. Integration of machine learning algorithms with experimental data will aid in identifying novel derivatives with enhanced pharmacological profiles. Furthermore, exploration of its role in precision medicine could lead to personalized therapeutic strategies tailored to individual patient needs.
In conclusion,2-Methoxy Phenothiazine represents a fascinating compound with diverse applications across multiple scientific disciplines. Its unique structural features and versatile biological activities make it an invaluable scaffold for drug discovery and development. As research continues to uncover new aspects of its pharmacological potential,2-Methoxy Phenothiazine is poised to play an increasingly significant role in addressing global health challenges through innovative chemical solutions.
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