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[2.2.1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)-
Time of Update: 2023-05-16
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is to use a sequence of reactions such as Suzuki-Miyaura coupling, hydroboration-oxidation, and Pd/C-mediated 5-Azaspiro[2.
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is to use a sequence of reactions such as Suzuki-Miyaura coupling, hydroboration-oxidation, and Pd/C-mediated 5-Azaspiro[2.
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The Instruction of 5-Azaspiro[2.4]heptane, 6-[5-[7-[2-(1R,3S,4S)-2-azabicyclo[2.2.1]hept-3-yl-1H
Time of Update: 2023-05-16
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a novel chemical compound that has recently gained attention in the scientific community for its unique properties and potential applications.
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a novel chemical compound that has recently gained attention in the scientific community for its unique properties and potential applications.
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The Synthetic Routes of 5-Azaspiro[2.4]heptane, 6-[5-[7-[2-(1R,3S,4S)-2-azabicyclo[2.2.1]hept-3-yl
Time of Update: 2023-05-16
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a synthetic compound that has a unique structure and possesses potential pharmacological properties.
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a synthetic compound that has a unique structure and possesses potential pharmacological properties.
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The Production Process of 5-Azaspiro[2.4]heptane, 6-[5-[7-[2-(1R,3S,4S)-2-azabicyclo[2.2.1]hept-3
Time of Update: 2023-05-16
The synthesis of this molecule involves a series of chemical reactions that require a high degree of stereochemical control to ensure the correct configuration of the final product.
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The Safety of 5-Azaspiro[2.4]heptane, 6-[5-[7-[2-(1R,3S,4S)-2-azabicyclo[2.2.1]hept-3-yl-1H
Time of Update: 2023-05-16
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a chemical compound that has been widely used in various industrial applications due to its unique properties.
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is a chemical compound that has been widely used in various industrial applications due to its unique properties.
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The Applications of 5-Azaspiro[2.4]heptane, 6-[5-[7-[2-(1R,3S,4S)-2-azabicyclo[2.2.1]hept-3-yl-1H
Time of Update: 2023-05-16
2. 1]hept-3-yl-1H-benzimidazol-6-yl]-9,9-difluoro-9H-fluoren-2-yl]-1H-imidazol-2-yl]-, hydrochloride (1:4), (6S)- is an organic compound that has been widely studied in the chemical industry due to its unique properties and diverse range of applications.
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The Safety of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
Time of Update: 2023-05-02
However, it is important to note that the potential for environmental harm from 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) is generally low, and it is not considered to be particularly harmful to the environment.
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The Synthetic Routes of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
Time of Update: 2023-05-02
Another common synthetic route of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) involves the following steps: Synthesis of 2H-Indol-2-one: This compound is synthesized by heating indole with hydrochloric acid.
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The Upstream and Downstream products of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1
Time of Update: 2023-05-02
The specific chemical products derived from this compound are proprietary information and are 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) is a unique compound with a wide range of applications in the chemical industry.
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The Instruction of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
Time of Update: 2023-05-02
Toxicity and Side Effects: The toxicity and side effects of 2H-Indol-2-one, 5-[2-[4-(1,2 Introduction:2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) is a novel drug candidate that has shown promise in the treatment of various diseases, including cancer and neurological disorders.
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The Applications of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
Time of Update: 2023-05-02
Pharmaceuticals: The compound, 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) is used as a starting material in the synthesis of new drugs.
Pharmaceuticals: The compound, 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) is used as a starting material in the synthesis of new drugs.
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The Production Process of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1)
Time of Update: 2023-05-02
The next step in the production process of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) involves a condensation reaction between the starting materials prepared in step 1.
The next step in the production process of 2H-Indol-2-one, 5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1,3-dihydro-, hydrochloride, hydrate (1:1:1) involves a condensation reaction between the starting materials prepared in step 1.