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2-(2-BroMobenzyloxy)aniline hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97026-25-0

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97026-25-0 Usage

General Description

2-(2-Bromobenzyloxy)aniline hydrochloride is a chemical compound with the molecular formula C13H14BrNO?HCl. It is a crystalline solid that is used in the synthesis of pharmaceuticals and other organic compounds. 2-(2-BroMobenzyloxy)aniline hydrochloride is a derivative of aniline and contains a bromobenzyloxy group, which makes it useful in organic chemistry reactions. It is typically found in the form of a white to off-white powder and is soluble in water and common organic solvents. The hydrochloride salt form of 2-(2-BroMobenzyloxy)aniline hydrochloride enhances its stability and solubility, making it easier to handle and use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 97026-25-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,0,2 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97026-25:
(7*9)+(6*7)+(5*0)+(4*2)+(3*6)+(2*2)+(1*5)=140
140 % 10 = 0
So 97026-25-0 is a valid CAS Registry Number.

97026-25-0SDS

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 Benzenamine, 2-[(2-bromophenyl)methoxy]-, hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(2-Bromobenzyloxy)aniline hydrochloride

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:97026-25-0 SDS

97026-25-0Downstream Products

97026-25-0Relevant academic research and scientific papers

An efficient assembly of heterobenzazepine ring systems utilizing an intramolecular palladium-catalyzed cycloamination

Margolis, Brandon J.,Swidorski, Jacob J.,Rogers, Bruce N.

, p. 644 - 647 (2003)

Azaheterocyclic compounds are interesting and medicinally relevant targets. Herein we disclose an improved synthesis into the oxazepine and thiazepine ring systems. The key step in the synthesis exploits recent advancements in the palladium-catalyzed amination reaction, which was utilized to form the seven-membered rings. General conditions for this reaction were Pd2dba3, P(t-Bu)3, NaO-t-Bu alone or with K2CO3, in toluene. The scope of the reaction was investigated, and has been shown to be effective on a variety of substrates as illustrated.

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