1006865-32-2

Basic information

• Product Name: (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene
• Synonyms: (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene;Benzene,1-bromo-4-[[(2S)-3-methoxy-2-methylpropoxy]methyl]-;1-Bromo-4-[[(2S)-3-methoxy-2-methylpropoxy]methyl]benzene
• CAS NO: 1006865-32-2
• Molecular Formula: C₁₂H₁₇BrO₂
• Molecular Weight: 273.16618
• Product Categories: API intermediates
• Mol File: 1006865-32-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 313.55 °C at 760 mmHg
• Flash Point: 124.135 °C
• Appearance: cream
• Density: 1.256 g/cm³
• CAS DataBase Reference: (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene(1006865-32-2)
• EPA Substance Registry System: (S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene(1006865-32-2)

Safety Data

• Hazardous Substances Data: 1006865-32-2(Hazardous Substances Data)

Usage

General Description

"(S)-1-Bromo-4-((3-methoxy-2-methylpropoxy)methyl)benzene" is a complex chemical compound exploring structure-dependent nature implicitly. It consists of a benzenic base and has bromine, methoxy, and methylpropoxy groups attached to it. The presence of the chiral center, as represented by the (S)-marker, highlights its optical behavior in chemical reactions. The bromine atom adds halogenic properties while the methoxy and methylpropoxy substructures provide etheric characteristics. Exact physical properties, reactivity or potential uses of this specific compound are not specified in the question, but it is clear that this molecule could potentially have a wide range of chemical reactivity due to its varied functional groups.

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

• 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 
• 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 
• 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 articles and documents

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

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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

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