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1059625-69-2

2,4,6-tribromobenzenediazonium 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1059625-69-2

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1059625-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1059625-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,9,6,2 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1059625-69:
(9*1)+(8*0)+(7*5)+(6*9)+(5*6)+(4*2)+(3*5)+(2*6)+(1*9)=172
172 % 10 = 2
So 1059625-69-2 is a valid CAS Registry Number.

1059625-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tribromobenzenediazonium tosylate

1.2 Other means of identification

Product number -
Other names 2,4,6-tribromobenzenediazonium 4-methylbenzenesulfonate

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:1059625-69-2 SDS

1059625-69-2Downstream Products

1059625-69-2Relevant articles and documents

Unusually stable, versatile, and pure arenediazonium tosylates: Their preparation, structures, and synthetic applicability

Filimonov, Victor D.,Trusova, Marina,Postnikov, Pavel,Krasnokutskaya, Elena A.,Lee, Young Min,Hwang, Ho Yun,Kim, Hyunuk,Chi, Ki-Whan

supporting information; experimental part, p. 3961 - 3964 (2009/05/30)

(Graph Presented) A new, simple, and effective method for the diazotization of a wide range of arylamines has been developed by using a polymer-supported diazotization agent in the presence of p-toluenesulfonic acid. Various pure arenediazonium tosylates with unusual stabilities can be easily prepared by this method. As a result, these salts are useful and versatile substrates for subsequent transformations, such as halogenation and Heck-type reactions. The unusual stabilities of arenediazonium tosylates are also preliminarily discussed with their X-ray structures.

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