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N-[4-(2-BROMO-ETHOXY)-PHENYL]-ACETAMIDE is a chemical compound that features a phenyl ring with a bromo-ethoxy group attached and an acetamide functional group. It is utilized in organic chemistry as a building block for synthesizing more complex molecules and may have potential applications in pharmaceuticals and agrochemicals due to its structural attributes.

57011-90-2

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57011-90-2 Usage

Uses

Used in Organic Chemistry:
N-[4-(2-BROMO-ETHOXY)-PHENYL]-ACETAMIDE is used as a building block for the synthesis of more complex molecules, contributing to the development of advanced chemical compounds.
Used in Pharmaceutical Development:
N-[4-(2-BROMO-ETHOXY)-PHENYL]-ACETAMIDE is used as a potential candidate in the development of pharmaceuticals, owing to its unique structural features that may offer therapeutic benefits.
Used in Agrochemical Development:
N-[4-(2-BROMO-ETHOXY)-PHENYL]-ACETAMIDE is used as a potential component in the development of agrochemicals, potentially contributing to the creation of new pesticides or other agricultural products.
Safety Precautions:
It is important to handle N-[4-(2-BROMO-ETHOXY)-PHENYL]-ACETAMIDE with care and follow proper safety precautions due to the potential hazards associated with its bromo-ethoxy group.

Check Digit Verification of cas no

The CAS Registry Mumber 57011-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,1 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57011-90:
(7*5)+(6*7)+(5*0)+(4*1)+(3*1)+(2*9)+(1*0)=102
102 % 10 = 2
So 57011-90-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12BrNO2/c1-8(13)12-9-2-4-10(5-3-9)14-7-6-11/h2-5H,6-7H2,1H3,(H,12,13)

57011-90-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(2-Bromo-ethoxy)-phenyl]-acetamide

1.2 Other means of identification

Product number -
Other names atiprosin

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:57011-90-2 SDS

57011-90-2Relevant academic research and scientific papers

A sustainable self-reproducing liposome consisting of a synthetic phospholipid

Matsuo, Muneyuki,Ohyama, Shota,Sakurai, Kotoba,Toyota, Taro,Suzuki, Kentaro,Sugawara, Tadashi

, p. 1 - 7 (2019)

A novel phosphoric membrane lipid (phospholipid) bearing an oleyl group as one of the hydrophobic chains formed a liposome with a thin lamella in water. Since the anionic membrane of pre-existing liposomes acted as a catalytic surface in phosphate buffer,

Derivatization of methylglyoxal for LC-ESI-MS analysis—stability and relative sensitivity of different derivatives

Fritzsche, Stefan,Billig, Susan,Rynek, Robby,Abburi, Ramarao,Tarakhovskaya, Elena,Leuner, Olga,Frolov, Andrej,Birkemeyer, Claudia

, (2018)

The great research interest in the quantification of reactive carbonyl compounds (RCCs), such as methylglyoxal (MGO) in biological and environmental samples, is reflected by the fact that several publications have described specific strategies to perform

NITRIC OXIDE RELEASING DERIVATIVES OF PARACETAMOL

-

Page/Page column 5, (2010/09/18)

The present invention particularly relates to novel nitrate esters of paracetamol. The nitrate esters of paracetamol are prepared by reacting the paracetamol with dihaloalkyl compound and followed by reaction with silver nitrate to obtain the correspondin

NITRIC OXIDE RELEASING DERIVATIVES OF PARACETAMOL

-

Page/Page column 10-11, (2009/04/25)

The present invention particularly relates to novel nitrate esters of paracetamol. The nitrate esters of paracetamol are prepared by reacting the paracetamol with dihaloalkyl compound and followed by reaction with silver nitrate to obtain the correspondin

Development of a selective ESI-MS derivatization reagent: Synthesis and optimization for the analysis of aldehydes in biological mixtures

Eggink, Mark,Wijtmans, Maikel,Ekkebus, Reggy,Lingeman, Henk,De Esch, Iwan J. P.,Kool, Jeroen,Niessen, Wilfried M. A.,Irth, Hubertus

experimental part, p. 9042 - 9051 (2009/06/06)

In LC-MS, derivatization is primarily used to improve ionization characteristics, especially for analytes that are not (efficiently) ionized by ESI or APCI such as aldehydes, sugars, and steroids. Derivatization strategies are then directed at the incorporation of a group with a permanent charge. A compound class that typically requires derivatization prior to LC-MS is the group of small aliphatic aldehydes that are, for instance, analyzed as the key biomarkers for lipid peroxidation in organisms. Here we report the development of a new tailor-made, highly sensitive, and selective derivatization agent 4-(2-(trimethylammonio)ethoxy)benzenaminium halide (4-APC) for the quantification of aldehydes in biological matrixes with positive ESI-MS/MS without additional extraction procedures. 4-APC possesses an aniline moiety for a fast selective reaction with aliphatic aldehydes as well as a quaternary ammonium group for improved MS sensitivity. The derivatization reaction is a convenient one-pot reaction at a mild pH (5.7) and temperature (10°C). As a result, an in-vial derivatization can be performed before analysis with an LC-MS/MS system. All aldehydes are derivatized within 30 min to a plateau, except malondialdehyde, which requires 300 min to reach a plateau. All derivatized aldehydes are stable for at least 35 h. Linearity was established between 10 and 500 nM and the limits of detection were in the 3-33 nM range for the aldehyde derivatives. Furthermore, the chosen design of these structures allows tandem MS to be used to monitor the typical losses of 59 and 87 from aldehyde derivatives, thereby enabling screening for aldehydes. Finally, of all aldehydes, pentanal and hexanal were detected at elevated levels in pooled healthy human urine samples.

A multi-mode-driven molecular shuttle: Photochemically and thermally reactive azobenzene rotaxanes

Murakami, Hiroto,Kawabuchi, Atsushi,Matsumoto, Rika,Ido, Takeshi,Nakashima, Naotoshi

, p. 15891 - 15899 (2007/10/03)

The shuttling process of α-CyD in three rotaxanes (1-3) containing α-cyclodextrin (α-CyD) as a ring, azobenzene as a photoactive group, viologen as an energy barrier for slipping of the ring, and 2,4-dinitrobenzene as a stopper was investigated. The trans

Preparation and Characterization of Base-Sensitive Destructible Surfactants

Jaeger, David A.,Finley, C. Timothy,Walter, Mark R.,Martin, Craig A.

, p. 3956 - 3959 (2007/10/02)

Destructible surfactants 4-n-C12H25C6H4SO2CH2CH2OC6H4X-4 (1, X = N+Me3, NO3-; 2, X = SO3-, K+) were prepared, and their stability/lability characteristics in aqueous micellar solutions with respect to E1cB elimination to give 4-n-C12H25C6H4SO2CH=CH2 (7) and HOC6H4X-4 (8/9) were determined by 1H NMR.In 0.001 and 0.1 M DCl, both 1 and 2 were stable for 24 h at 75 deg C.In D2O alone at 25 deg C, 1 slowly decomposed, and 2 was stable.At 25 deg C, 1 decomposed completely within 10 min in 0.1 M NaHCO3, whereas 2 was more stable in 0.1 M K2CO3.The difference in reactivities for 1 and 2 was ascribed to a combination of electronic and micellar effects.Support for the latter was found in a comparison of 2's behavior with that of 4-MeC6H4SO2CH2CH2OC6H4SO3Na-4 (10).

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