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5-butylphenanthridinium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118664-90-7

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118664-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118664-90-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,6 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118664-90:
(8*1)+(7*1)+(6*8)+(5*6)+(4*6)+(3*4)+(2*9)+(1*0)=147
147 % 10 = 7
So 118664-90-7 is a valid CAS Registry Number.

118664-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-butylphenanthridin-5-ium,bromide

1.2 Other means of identification

Product number -
Other names 5-butylphenanthridin-5-ium bromide

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:118664-90-7 SDS

118664-90-7Downstream Products

118664-90-7Relevant academic research and scientific papers

Copper-Catalyzed Annulation: A Method for the Systematic Synthesis of Phenanthridinium Bromide

Jhang, Yuan-Ye,Fan-Chiang, Tai-Ting,Huang, Jun-Min,Hsieh, Jen-Chieh

, p. 1154 - 1157 (2016/03/15)

A novel procedure for the Cu-catalyzed systematic synthesis of phenanthridinium bromide is reported. This transformation was achieved with direct construction of central pyridinium core by using an in situ formed biaryl imine as a substrate. Tolerance of a very wide variety of N-substituents is indicated; this has never previously been disclosed by other reports. Application of this method to synthesis of the natural alkaloid bicolorine, and its derivatives, was also carried out in only three synthetic steps from commercially available compounds.

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