-
The Upstream and Downstream products of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
Cimetidine is a medication that is used to treat certain types of ulcers and to reduce the amount of acid produced in the stomach.
Cimetidine is a medication that is used to treat certain types of ulcers and to reduce the amount of acid produced in the stomach.
-
The Synthetic Routes of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is an important intermediate in the production of various chemicals and pharmaceuticals.
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is an important intermediate in the production of various chemicals and pharmaceuticals.
-
The Production Process of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is a complex chemical synthesis that involves several steps and requires a high degree of technical expertise.
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is a complex chemical synthesis that involves several steps and requires a high degree of technical expertise.
-
The Applications of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is a chemical compound with a unique structure and properties that make it a versatile building block in the chemical industry.
-
The Safety of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is a hazardous substance that requires careful handling to prevent harm to workers and the environment.
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- is a hazardous substance that requires careful handling to prevent harm to workers and the environment.
-
The Instruction of 8-Azabicyclo[3.2.1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)-
Time of Update: 2023-05-18
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- has several uses in the chemical industry, including the following: Pharmaceuticals The unique chemical properties of 8-Azabicyclo[3.
2. 1]octane-3-thiol, 8-methyl-, hydrochloride (1:1), (3-exo)- has several uses in the chemical industry, including the following: Pharmaceuticals The unique chemical properties of 8-Azabicyclo[3.
-
The Synthetic Routes of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
2. 1]octane involves the use of a Pd/C catalyzed coupling reaction between 3-methyl-5-(1-methylethyl)-4H-1,2,4-triazole and 8-phenylmethyl-8-azabicyclo[3.
2. 1]octane involves the use of a Pd/C catalyzed coupling reaction between 3-methyl-5-(1-methylethyl)-4H-1,2,4-triazole and 8-phenylmethyl-8-azabicyclo[3.
2. 1]octane involves the use of a Pd/C catalyzed coupling reaction between 3-methyl-5-(1-methylethyl)-4H-1,2,4-triazole and 8-phenylmethyl-8-azabicyclo[3.
-
The Instruction of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
One commonly used synthesis route involves the following steps: Preparation of the starting material: This involves the synthesis of the intermediate compound 3-[2-(1H-1,2,4-Triazol-1-yl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepin-9-yl]-N-phenyl-acetamide, which can be synthesized using known methods such as reported in the literature.
-
The Safety of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
This includes the proper storage of raw materials, the use of appropriate safety equipment, and the implementation of waste management protocols to ensure that any potential releases of the chemical are managed in a safe and responsible manner.
-
The Production Process of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
Chemical reactions involved in the production process The production process of R218 involves several chemical reactions, including the following: Synthesis of tetrabutylammonium iodide: Tetrabutylammonium iodide is synthesized by reacting tetrabutylammonium hydroxide with iodine in the presence of a solvent such as water or methanol.
-
The Applications of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
Its potential use in the treatment of various diseases and in the development of new chemicals make it an important compound in the field of chemical engineering.
-
The Upstream and Downstream products of (3-exo)-3-[3-Methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-(phenylmethyl)-8-azabicyclo[3.2.1]octane
Time of Update: 2023-05-13
The chemical industry plays a key role in the development and production of antiviral agents like ABT-398, ensuring that these treatments are safe and effective for use in treating a variety of diseases.
-
exo-selective intermolecular Diels-Alder reaction enzyme in nature
Time of Update: 2021-12-28
Words for Java 18. 9" >Pharmaceutical intermediates, pesticides and fine chemicals occupy an important position in the national economy and people's livelihood . Traditional chemical synthesis proce
-
Is Israel's new drug EXO-CD24 the hope of ending the new coronavirus?
Time of Update: 2021-08-28
The main reason for the death of patients with the new coronavirus infection is the strong pulmonary immune response-or cytokine storm .
-
ATVB: Lower HDL cholesterol levels were associated with higher exo-white blood cell counts
Time of Update: 2021-01-01
In genetic analysis using anti-variance weighted analysis for age and gender correction, genetically determined HDL cholesterol decreased by 1mmol/L (39 mg/dL) and white blood cells increased by 2.2% (95% CI by 0.3% to 4.1%), and lymphocytes increased by 4.3%.