1006865-32-2

Usage

Uses

Given the lack of specific applications in the provided materials, the potential uses of (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene can only be hypothesized based on its structural features. Here are some possible applications across different industries:
Used in Pharmaceutical Industry:
(S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene could be used as an intermediate in the synthesis of pharmaceutical compounds due to its unique structural features, including the bromine atom and etheric groups, which may be involved in the formation of new drugs with specific therapeutic properties.
Used in Chemical Synthesis:
In the field of organic chemistry, (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene might serve as a building block or reactant in the synthesis of more complex molecules, leveraging its halogenic and etheric properties for various chemical reactions.
Used in Material Science:
(S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene's structural components could potentially be utilized in the development of new materials with specific properties, such as improved solubility, stability, or reactivity, depending on the requirements of the material science industry.
Used in Agrochemical Industry:
Given its halogenic nature, (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene might find applications in the agrochemical sector, possibly as a precursor for the development of new pesticides or herbicides with targeted effects on pests or weeds.

Upstream product

• 1147886-64-3 (S)-3-(4-bromo-benzyloxy)-2-methyl-propan-1-ol 
• 74-88-4 methyl iodide 
• 1018349-44-4 3-(4-bromo-benzyloxy)-2-methyl-propionic acid methyl ester 
• 911855-78-2 (R)-3-methoxy-2-methyl-propan-1-ol 
• 589-17-3 p-bromobenzyl chloride 

Downstream Products

• 1247088-34-1 C₃₄H₄₄N₂O₄ 
• 1366039-59-9 C₃₉H₅₂N₂O₆ 
• 1018478-38-0 (3R,4R,5S)-1-benzyl-3-hydroxy-4-[4-((S)-3-methoxy-2-methyl-propoxymethyl)-phenyl]-5-trityloxymethyl-piperidinium (S)-carboxy-phenyl-methanolate 
• 1006901-40-1 1-benzyl-4-[4-((S)-3-methoxy-2-methyl-propoxymethyl)-phenyl]-5-trityloxymethyl-piperidin-3-ol 
• 1006865-29-7 (rac-3R,4R,5S)-1-benzyl-4-[4-((S)-3-methoxy-2-methyl-propoxymethyl)-phenyl]-5-trityloxymethyl-piperidin-3-ol 
• 1006865-30-0 1-benzyl-4-[4-((S)-3-methoxy-2-methyl-propoxy-methyl)-phenyl]-3-(R,S)-trityloxymethyl-1,2,3,6-tetrahydro-pyridine 
• 1017578-39-0 8-methoxycarbonylmethyl-7-[4-((S)-3-methoxy-2-methyl-propoxymethyl)-phenyl]-9-methyl-3,9-diaza-bicyclo[3.3.1]non-6-ene-3-carboxylic acid tert-butyl ester 
• 1006865-31-1 1-benzyl-4-[4-((S)-3-methoxy-2-methyl-propoxymethyl)-phenyl]-3-(R,S)-trityloxy-methyl-piperidin-4-(R,S)-ol 

Relevant academic research and scientific papers

3,4-Diarylpiperidines as potent renin inhibitors

The discovery and SAR of a series of potent renin inhibitors possessing a novel 3,4-diarylpiperidine scaffold are described herein. The resulting compound 38 exhibit low nanomolar plasma renin IC50, had a clean CYP 3A4 profile and displayed mic

TRISUBSTITUTED PIPERIDINES

The application relates to trisubstituted piperidines of the general formula (I) and their salts, preferably their pharmaceutically acceptable salts, in which R1, R2, R3 and X have the meanings explained in the description

4,4-DISUBSTITUTED PIPERIDINES

The application relates to 4,4-disubstituted piperidines of the general formula (I) and their salts, preferably their pharmaceutically acceptable salts, in which R2, has the meanings explained in the description, a process for their preparation

SUBSTITUTED PIPERIDINES AS THERAPEUTIC COMPOUNDS

Described are compounds of the general formula (I), and pharmaceutically acceptable salt thereof, in which R1 has the definitions illustrated in detail in the description, as beta-secretase, cathepsin D, plasmepsin II and/or HIV protease inhibi

Phenyl piperidine derivatives for use as renin inhibitors

Compounds of the general formula and the salts thereof, preferably the pharmaceutically acceptable salts thereof; in which R1 is straight-chain C1-8-alkanoyloxy, straight-chain C1-8-alkoxy, straight-chain C1-8-a

Organic compounds

The present invention relates to substituted piperidines of the general formula (I), where R1, R2, R3, R4, R5, Q and X have the definitions elucidated in more detail in the description, to a process for their preparation and to the use of these compounds as medicines, in particular as renin inhibitors. Moreover, the enzymatic substrate portion of the compound is simultaneously a substrate for a membrane transporter.

Tetrahydropyridines as renin inhibitors

The application relates to novel substituted tetrahydropyridines of the general formulae (I) and (II) and the salts thereof, preferably the pharmaceutically acceptable salts thereof, in which Q, T, V and W have the meanings defined in the description, to

NITRATE ESTERS OF PIPERIDINES

The application relates to novel nitrate ester derivatives of substituted piperidines of the general formula (I), wherein R1, R2, R3, X, Y and Z0, and m, n, p and q have the meanings explained in more detail in