4125-32-0

Basic information

• Product Name: 1-Methoxy-4-(1-Methylbutyl)benzene
• Synonyms: 1-Methoxy-4-(1-Methylbutyl)benzene
• CAS NO: 4125-32-0
• Molecular Formula: C₁₂H₁₈O
• Molecular Weight: 178.27072
• Product Categories: Aromatics, Miscellaneous Reagents
• Mol File: 4125-32-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Methoxy-4-(1-Methylbutyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methoxy-4-(1-Methylbutyl)benzene(4125-32-0)
• EPA Substance Registry System: 1-Methoxy-4-(1-Methylbutyl)benzene(4125-32-0)

Safety Data

• Hazardous Substances Data: 4125-32-0(Hazardous Substances Data)

Usage

Description

1-Methoxy-4-(1-Methylbutyl)benzene, also known as an alkylphenol derivative, is an organic compound characterized by the presence of a methoxy group and a methylbutyl group attached to a benzene ring. It is known for its potential applications in various industries due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
1-Methoxy-4-(1-Methylbutyl)benzene is used as a synthetic intermediate for the production of alkylphenols with biological activity. These alkylphenols are essential in the development of pharmaceutical compounds, particularly those with potential therapeutic applications.
Used in Chemical Synthesis:
1-Methoxy-4-(1-Methylbutyl)benzene serves as a key building block in the synthesis of various organic compounds, including those with applications in the chemical, material science, and pharmaceutical industries. Its unique structure allows for further functionalization and modification to create a wide range of products with specific properties and applications.

Upstream product

• 107-81-3 2-bromopentane 
• 66107-29-7 4-methoxyphenyl triflate 
• 109-66-0 pentane 
• 91763-97-2 2-(4-Methoxy-phenyl)-pentanol-⁽²⁾ 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 7152-03-6 p-methoxyphenyl cyclopropyl ketone 
• 74-88-4 methyl iodide 
• 829-17-4 1‐(1‐cyclopropylvinyl)‐4‐methoxybenzene 
• 17404-06-7 (E)-2-(4-methoxyphenyl)pent-2-ene 
• 504-60-9 penta-1,3-diene 
• 578-57-4 2-bromoanisole 

Downstream Products

• 4097-42-1 2-<4-Hydroxy-3,5-dinitro-phenyl>-pentan 
• 100-09-4 4-methoxybenzoic acid 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 

Relevant articles and documents

Terminal-Selective Functionalization of Alkyl Chains by Regioconvergent Cross-Coupling

Hydrocarbons are still the most important precursors of functionalized organic molecules, which has stirred interest in the discovery of new C?H bond functionalization methods. We describe herein a new step-economical approach that enables C?C bonds to be constructed at the terminal position of linear alkanes. First, we show that secondary alkyl bromides can undergo in situ conversion into alkyl zinc bromides and regioconvergent Negishi coupling with aryl or alkenyl triflates. The use of a suitable phosphine ligand favoring Pd migration enabled the selective formation of the linear cross-coupling product. Subsequently, mixtures of secondary alkyl bromides were prepared from linear alkanes by standard bromination, and regioconvergent cross-coupling then provided access to the corresponding linear arylation product in only two steps.

The action of sodium hydrogen telluride on olefins

The action of sodium hydrogen telluride, NaTeH, on non electrophilic carbon-arbon double bonds has been investigated.The reaction is found to be very sensitive to the substituents on the ethylenic linkage. Whereas phenyl conjugated olefins are reduced to alkylbenzenes,the reagent adds to isolated mono and disubstituted double bonds leading to organotellurium derivatives and with gem-disubstituted ones it leads to a mixture of reduction and addition products. These results are interpreted in terms of a radical pair mechanism involving hydrogen atom transfer from hydrogen telluride,HTe- to the double bond.

Structures and pesticidal activities of derivatives of dinitro-phenols. IV. Preparation of certain 2-(alpha-branched alkyl)-4,6-dinitro- and 4-(alpha-branched alkyl)-2,6-dinitro-phenols.

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