What is the 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-?

10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- is , while it's Molecular Formula is C20H14ClNO2S. Used in Medicinal Chemistry: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used as a research compound for exploring its potential biological activities. The presence of the chlorine atom and the 4-methoxybenzoyl group may enhance or modulate the compound's therapeutic effects, making it a valuable tool in the development of new drugs. Used in Pharmaceutical Industry: In the pharmaceutical industry, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used as a lead compound for the development of novel therapeutic agents. Its potential as an anti-inflammatory, antipsychotic, and anti-tumor agent makes it a promising candidate for the treatment of various diseases and conditions. Used in Drug Discovery and Development: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is utilized in drug discovery and development processes to identify new molecular targets and pathways for therapeutic intervention. Its unique structural features and potential biological activities make it a valuable asset in the search for innovative treatments. Used in Chemical Research: In chemical research, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)serves as a model compound for studying the structure-activity relationships of phenothiazine derivatives. Understanding how the 2-chloro-10-(4-methoxybenzoyl)substitution pattern affects the compound's properties can provide insights into the design of more effective and targeted therapeutic agents. Used in Biochemical Studies: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is employed in biochemical studies to investigate its interactions with various biological targets, such as enzymes, receptors, and signaling pathways. This information can help elucidate the compound's mechanism of action and guide the optimization of its therapeutic potential. Used in Toxicological Assessments: In toxicological assessments, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used to evaluate its safety profile and potential side effects. Understanding the compound's toxicological properties is crucial for ensuring its safe use in medical applications. Used in Drug Synthesis: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is utilized in drug synthesis processes to produce novel analogs and derivatives with improved pharmacological properties. The synthesis of these compounds can lead to the development of more effective and safer therapeutic agents. Used in Drug Formulation: In drug formulation, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used to develop pharmaceutical formulations with optimal drug delivery and bioavailability. 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-'s physicochemical properties can be tailored to enhance its performance in various dosage forms. Used in Clinical Trials: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)may be used in clinical trials to evaluate its efficacy and safety in treating specific diseases or conditions. These trials are essential for determining the compound's potential as a viable therapeutic option. Used in Regulatory Approval Processes: In regulatory approval processes, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is subjected to rigorous evaluation by regulatory agencies to ensure its safety, efficacy, and quality for medical use. Successful approval can pave the way for the compound's commercialization and availability to patients in need.

What is the CAS number for 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-?

The CAS number of 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- is 105925-39-1.

What is 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- (105925-39-1) used for?

10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-, is a chemical compound with the molecular formula C18H14ClNO2. It is a derivative of phenothiazine, featuring a chlorine atom and a 4-methoxybenzoyl group. 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)has potential applications in medicinal chemistry due to the diverse biological activities of phenothiazine derivatives, such as anti-inflammatory, antipsychotic, and anti-tumor properties. The specific 2-chloro-10-(4-methoxybenzoyl)substitution pattern may influence the compound's chemical and biological characteristics, making it a promising candidate for further research and development.

What is the 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-?

10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- is , while it's Molecular Formula is C20H14ClNO2S. Used in Medicinal Chemistry: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used as a research compound for exploring its potential biological activities. The presence of the chlorine atom and the 4-methoxybenzoyl group may enhance or modulate the compound's therapeutic effects, making it a valuable tool in the development of new drugs. Used in Pharmaceutical Industry: In the pharmaceutical industry, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used as a lead compound for the development of novel therapeutic agents. Its potential as an anti-inflammatory, antipsychotic, and anti-tumor agent makes it a promising candidate for the treatment of various diseases and conditions. Used in Drug Discovery and Development: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is utilized in drug discovery and development processes to identify new molecular targets and pathways for therapeutic intervention. Its unique structural features and potential biological activities make it a valuable asset in the search for innovative treatments. Used in Chemical Research: In chemical research, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)serves as a model compound for studying the structure-activity relationships of phenothiazine derivatives. Understanding how the 2-chloro-10-(4-methoxybenzoyl)substitution pattern affects the compound's properties can provide insights into the design of more effective and targeted therapeutic agents. Used in Biochemical Studies: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is employed in biochemical studies to investigate its interactions with various biological targets, such as enzymes, receptors, and signaling pathways. This information can help elucidate the compound's mechanism of action and guide the optimization of its therapeutic potential. Used in Toxicological Assessments: In toxicological assessments, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used to evaluate its safety profile and potential side effects. Understanding the compound's toxicological properties is crucial for ensuring its safe use in medical applications. Used in Drug Synthesis: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is utilized in drug synthesis processes to produce novel analogs and derivatives with improved pharmacological properties. The synthesis of these compounds can lead to the development of more effective and safer therapeutic agents. Used in Drug Formulation: In drug formulation, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is used to develop pharmaceutical formulations with optimal drug delivery and bioavailability. 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-'s physicochemical properties can be tailored to enhance its performance in various dosage forms. Used in Clinical Trials: 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)may be used in clinical trials to evaluate its efficacy and safety in treating specific diseases or conditions. These trials are essential for determining the compound's potential as a viable therapeutic option. Used in Regulatory Approval Processes: In regulatory approval processes, 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)is subjected to rigorous evaluation by regulatory agencies to ensure its safety, efficacy, and quality for medical use. Successful approval can pave the way for the compound's commercialization and availability to patients in need.

What is the CAS number for 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-?

The CAS number of 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- is 105925-39-1.

What is 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)- (105925-39-1) used for?

10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)-, is a chemical compound with the molecular formula C18H14ClNO2. It is a derivative of phenothiazine, featuring a chlorine atom and a 4-methoxybenzoyl group. 10H-Phenothiazine, 2-chloro-10-(4-methoxybenzoyl)has potential applications in medicinal chemistry due to the diverse biological activities of phenothiazine derivatives, such as anti-inflammatory, antipsychotic, and anti-tumor properties. The specific 2-chloro-10-(4-methoxybenzoyl)substitution pattern may influence the compound's chemical and biological characteristics, making it a promising candidate for further research and development.

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105925-39-1

Product Name:iHAP1
Molecular Formula:C20H14ClNO2S
Molecular Weight:367.856

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Product Details

Purity:99%

99% Purity Commercial production iHAP1 105925-39-1 with Cheapest Price

Molecular Formula:C20H14ClNO2S
Molecular Weight:367.856

105925-39-1 Relevant articles

Tricyclic phenothiazine and phenoselenazine derivatives as potential multi-targeting agents to treat Alzheimer's disease

Tin, Gary,Mohamed, Tarek,Gondora, Nyasha,Beazely, Michael A.,Rao, Praveen P. N.

, p. 1930 - 1941 (2015/11/17)

A group of tricyclic phenothiazines (6a,...

N-benzoylated phenoxazines and phenothiazines: Synthesis, antiproliferative activity, and inhibition of tubulin polymerization

Prinz, Helge,Chamasmani, Behfar,Vogel, Kirsten,B?hm, Konrad J.,Aicher, Babette,Gerlach, Matthias,Günther, Eckhard G.,Amon, Peter,Ivanov, Igor,Müller, Klaus

supporting information; experimental part, p. 4247 - 4263 (2011/08/05)

A total of 53 N-benzoylated phenoxazines...

105925-39-1 Process route

: 92-39-7
2-chlorophenothiazine

: 100-07-2
4-methoxy-benzoyl chloride

: 105925-39-1
2-chloro-10H-phenothiazin-10-yl-(4-methoxyphenyl)-methanone

Conditions

Conditions	Yield
In toluene; at 110 ℃;	94%
In toluene; Reflux;	65%

: 105925-39-1
2-chloro-10H-phenothiazin-10-yl-(4-methoxyphenyl)-methanone

Conditions

Conditions	Yield
aus Phenothiazin, d. Benzoylchlorid;

105925-39-1 Upstream products

92-39-7
2-chlorophenothiazine
100-07-2
4-methoxy-benzoyl chloride

105925-39-1 Downstream products

1309924-88-6
2-chloro-10-(4-methoxybenzoyl)-10H-phenothiazine-5-oxide

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