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3-(4-Bromophenoxy)-N,N-dimethylpropylamine is a chemical compound characterized by the molecular formula C12H18BrNO. It is a tertiary amine with a bulky N,N-dialkyl substituent, featuring a bromine atom attached to a phenyl ring and a dimethylpropylamine moiety. 3-(4-Bromophenoxy)-N,N-dimethylpropylamine is known for its versatility in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, making it a valuable asset in various chemical reactions as a catalyst or reagent. Its unique properties also suggest potential biological activity, positioning it as a candidate for applications in medicinal chemistry and drug discovery.

76579-64-1

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76579-64-1 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(4-Bromophenoxy)-N,N-dimethylpropylamine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of complex molecular structures. Its presence in the synthesis process can enhance the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Production:
In the agrochemical industry, 3-(4-Bromophenoxy)-N,N-dimethylpropylamine is utilized as a precursor in the production of various agrochemicals, contributing to the development of more effective and targeted pest control agents.
Used as a Catalyst in Organic Reactions:
3-(4-Bromophenoxy)-N,N-dimethylpropylamine is employed as a catalyst in a range of organic reactions due to its ability to accelerate the reaction rate and improve the yield of desired products. Its tertiary amine nature allows it to participate in various catalytic cycles, making it a versatile component in organic synthesis.
Used in Medicinal Chemistry and Drug Discovery:
3-(4-Bromophenoxy)-N,N-dimethylpropylamine is used as a starting material or a building block in medicinal chemistry for the design and synthesis of novel bioactive compounds. Its potential biological activity and structural features make it a promising candidate for the development of new therapeutic agents.
Used in Chemical Research:
In the field of chemical research, 3-(4-Bromophenoxy)-N,N-dimethylpropylamine serves as a model compound for studying reaction mechanisms and exploring new synthetic methodologies. Its unique structural elements provide opportunities for researchers to investigate its reactivity and potential applications in various chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 76579-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76579-64:
(7*7)+(6*6)+(5*5)+(4*7)+(3*9)+(2*6)+(1*4)=181
181 % 10 = 1
So 76579-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16BrNO/c1-13(2)8-5-9-14-11-7-4-3-6-10(11)12/h3-4,6-7H,5,8-9H2,1-2H3

76579-64-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenoxy)-N,N-dimethylpropan-1-amine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76579-64-1 SDS

76579-64-1Relevant academic research and scientific papers

IMIDAZO[4,5-C]QUINOLIN-2-ONE COMPOUNDS AND THEIR USE IN TREATING CANCER

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Page/Page column 47, (2017/05/20)

The specification generally relates to compounds of Formula (I) and pharmaceutically acceptable salts thereof, where x, R1, R2, R3, R4 and R5 have any of the meanings defined herein. The specification also relates to the use of compounds of Formula (I) and salts thereof to treat or prevent ATM mediated disease, including cancer. The specification further relates to pharmaceutical compositions comprising substituted imidazo[4,5-c]quinolin-2-one compounds and pharmaceutically acceptable salts thereof; kits comprising such compounds and salts; methods of manufacture of such compounds and salts; and intermediates useful in such manufacture.

Solution-processed interlayer of discotic-based small molecules for organic photovoltaic devices: Enhancement of both the open-circuit voltage and the fill factor

Song, Ho Jun,Lee, Eui Jin,Kim, Doo Hun,Lee, Tae Ho,Goh, Munju,Lee, Sangkug,Moon, Doo Kyung

, p. 210 - 218 (2014/11/12)

A novel alcohol/water-soluble, discotic type derivative of pyrene was obtained using a simple synthesis process. The pyrene derivative was dissolved in organic solvents and highly polar solvents. The absorption spectrum of the pyrene derivative in a thin film was almost identical with that observed in solution compared with a fluorene derived co-polymer, the extensive planarity of the pyrene unit is invoked to rationalize this observation. According to an XRD measurement, a huge portion of the pyrene derivatives are arranged face-on in regard of the substrate due to their discotic structure. A photovoltaic device containing the pyrene derivative exhibited an open-circuit voltage of 0.73 V, current density of 14.6 mA/cm2, fill factor of 65.1% and a power conversion efficiency of 7.0%. The photovoltaic device with the pyrene derivative exhibited an improved fill factor compared with that of the fluorene co-polymer (60.7%) due to the discotic structure. An inverted photovoltaic device containing pyrene derivative showed a power conversion efficiency of 8.3%.

ELECTRON TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE USING THEREOF

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Paragraph 0094; 0095; 0096; 0097, (2016/10/09)

The present invention relates to an electron-transporting material represented by chemical formula 1, and to an organic electroluminescent device using the same. The electron-transporting material according to the present invention can easily transport electrons and exhibits stable luminosity in an organic electroluminescent device, thereby being useful for a flat panel and a device for a plastic display.COPYRIGHT KIPO 2016

Preparation of a new class of cleavable surfactants based on the silicon-carbon bond

Noronha, Glenn,Nguyen, Khanhlinh T.

, p. 4935 - 4938 (2007/10/03)

The ability of silicon to direct electrophiles to the ipso-position is used in developing a new class of cleavable amphiphiles containing an acid labile silicon-carbon (aromatic) bond. The synthesis of these amphiphiles is carried out in four steps to yie

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