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1823-62-7

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1823-62-7 Usage

Description

4-[2-N,N-Diethylethoxy]phenyl bromide is a chemical compound that belongs to the class of phenyl bromides. It is a derivative of phenyl bromide, with the addition of a diethylethoxy group at the 2-position of the phenyl ring. 4-[2-N,N-DIETHYLETHOXY]PHENYL BROMIDE is commonly used in organic synthesis and serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and materials. It also has the potential for use as a substrate for the synthesis of novel compounds with potential biological activity. Due to its halogenated nature, it is important to handle and use this compound with caution to avoid hazardous effects.

Uses

Used in Pharmaceutical Industry:
4-[2-N,N-Diethylethoxy]phenyl bromide is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-[2-N,N-Diethylethoxy]phenyl bromide is utilized as a precursor in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used in Material Science:
4-[2-N,N-Diethylethoxy]phenyl bromide is employed as a building block in material science for the development of new materials with specific properties, such as improved stability or reactivity in various applications.
Used in Organic Synthesis:
As a versatile chemical intermediate, 4-[2-N,N-Diethylethoxy]phenyl bromide is used in organic synthesis for the preparation of a wide range of organic compounds, including those with potential biological activity, thus contributing to the discovery of new chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 1823-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1823-62:
(6*1)+(5*8)+(4*2)+(3*3)+(2*6)+(1*2)=77
77 % 10 = 7
So 1823-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H18BrNO/c1-3-14(4-2)9-10-15-12-7-5-11(13)6-8-12/h5-8H,3-4,9-10H2,1-2H3

1823-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenoxy)-N,N-diethylethanamine

1.2 Other means of identification

Product number -
Other names [2-(4-Bromo-phenoxy)-ethyl]-diethyl-amine

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:1823-62-7 SDS

1823-62-7Relevant articles and documents

Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds

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, (2008/06/13)

The present invention relates to alkyne compounds of general formula I wherein the groups and residues A, B, W, X, Y, Z, R1 and R2 have the meanings given in claim 1. The invention further relates to pharmaceutical compositions containing at least one alkyne according to the invention. In view of their MCH-receptor antagonistic activity the pharmaceutical compositions according to the invention are suitable for the treatment of metabolic disorders and/or eating disorders, particularly obesity, bulimia, anorexia, hyperphagia and diabetes.

NOVEL ALKYNE COMPOUNDS HAVING AN MCH ANTAGONISTIC EFFECT AND MEDICAMENTS CONTAINING THESE COMPOUNDS

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Page/Page column 107, (2008/06/13)

The invention relates to alkyne compounds of general formula (I), in which groups and residues A, B, W, X, Y, Z, R1 and R2 have the meanings as cited in Claim 1. The invention also relates to medicaments containing at least one inventive alkyne. The MCH receptor antagonistic effect renders the inventive medicaments suitable for treating metabolic disorders and/or eating disorders, in particular, obesity, bulimia, anorexia, hyperphagia and diabetes.

Sila-Pharmaca, 34th communication [1]. Sila-analogues of triparanol and ethamoxytriphetol: Synthesis as well as pharmacological and toxicological properties

Tacke,Bentlage-Felten,Linoh,Magda

, p. 649 - 654 (2007/10/02)

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