916084-58-7

Usage

Uses

Used in Pharmaceutical Industry:
Ethanol, 2-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(triphenylmethyl)-3-piperidinylidene]-, 1-(4-methylbenzenesulfonate), (2Z)is used as a pharmaceutical intermediate for the synthesis of various drugs. The unique functional groups present in the compound may provide specific reactivity or selectivity in chemical reactions, enabling the production of novel pharmaceutical agents with potential therapeutic benefits.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, Ethanol, 2-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(triphenylmethyl)-3-piperidinylidene]-, 1-(4-methylbenzenesulfonate), (2Z)can be employed as a building block or reagent in the synthesis of complex organic molecules. Ethanol,
2-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(triphenylmethyl)-3-piperidin
ylidene]-, 1-(4-methylbenzenesulfonate), (2Z)-'s unique structure and functional groups may facilitate the formation of new chemical bonds or enable the construction of specific molecular architectures, contributing to the development of advanced materials or novel chemical entities.
Used in Research and Development:
Ethanol, 2-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(triphenylmethyl)-3-piperidinylidene]-, 1-(4-methylbenzenesulfonate), (2Z)can also be utilized in research and development settings to explore its chemical properties and potential applications. Ethanol,
2-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-(triphenylmethyl)-3-piperidin
ylidene]-, 1-(4-methylbenzenesulfonate), (2Z)may serve as a model system for studying the reactivity and selectivity of various functional groups, or it may be used to investigate the effects of structural modifications on the compound's properties and behavior. This research could lead to a better understanding of the underlying chemical principles and pave the way for the discovery of new applications or the optimization of existing ones.

Upstream product

• 916084-56-5 (Z)-4-(t-butyldimethylsilyloxy)-3-(2-hydroxyethylidene)-1-(triphenylmethyl)piperidine 
• 4124-41-8 p-toluenesulfonylanhydride 

Downstream Products

• 916084-57-6 (Z)-4-(t-butyldimethylsilyloxy)-3-{2-[4-(ethoxycarbonylmethyl)-1H-pyrazol-1-yl]ethylidene}-1-(triphenylmethyl)piperidine 

Relevant academic research and scientific papers

CYCLIC AMINE DERIVATIVE HAVING SUBSTITUTED ALKYL GROUP

A compound having the general formula (I), pharmacologically acceptable salts thereof or prodrugs thereof:[wherein R1 represents a hydrogen atom, a C1-C6 alkyl group which may be substituted, a C3-C6 cycloalkyl group which may be substituted, a C1-C6 alkoxy group which may be substituted or a C6-C10 aryl group which may be substituted;R2 represents a hydrogen atom, a halogen atom, a carboxy group, a C2-C7 alkoxycarbonyl group, a carbamoyl group, a cyano group, a C1-C6 alkyl group, a halogeno C1-C6 alkyl group, a C1-C6 alkyl group substituted by a heteroaryl group, a C1-C6 alkoxy group, a halogeno C1-C6 alkoxy group, a hydroxy C1-C6 alkyl group, a C2-C12 alkoxyalkyl group, a formyl group, a C2-C7 alkanoyl group, a C4-C7 cycloalkylcarbonyl group, a C2-C7 alkylcarbamoyl group, a di(C1-C6 alkyl)carbamoyl group, a group of formula R4—CO—CR5R6—(CH2)m—, a group of formula R7—CO—(CH2)l—N(R8)— or a sulfamoyl C1-C6 alkyl group;R3 represents a substituted C1-C6 alkyl group, a heterocyclyl group or a heterocyclyl group substituted with 1 to 5 substituents;X1, X2, X3, X4 and X5 each independently represents a hydrogen atom, a halogen atom, an amino group, a carboxy group, a carbamoyl group, a cyano group, a nitro group, a C1-C6 alkyl group, a halogeno C1-C6 alkyl group, a C1-C6 alkoxy group, or a halogeno C1-C6 alkoxy group; andn represents an integer of 0 to 2]

CYCLIC AMINE DERIVATIVE HAVING SUBSTITUTED ALKYL GROUP

Disclosed is a compound represented by the general formula (I) below, a pharmacologically acceptable salt thereof, or a prodrug thereof. [Chemical formula 1] (I) (In the formula, R1 represents a hydrogen atom, an optionally substituted C1