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2-benzyl-5-nitroisoquinolinium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57249-08-8

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57249-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57249-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,4 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57249-08:
(7*5)+(6*7)+(5*2)+(4*4)+(3*9)+(2*0)+(1*8)=138
138 % 10 = 8
So 57249-08-8 is a valid CAS Registry Number.

57249-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-5-nitroisoquinolin-2-ium,bromide

1.2 Other means of identification

Product number -
Other names N-Benzyl-5-nitroisochinoliniumbromid

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:57249-08-8 SDS

57249-08-8Relevant academic research and scientific papers

Base-promoted aerobic oxidation of: N -alkyl iminium salts derived from isoquinolines and related heterocycles

Bai, Li-Gang,Zhou, Yue,Zhuang, Xin,Zhang, Liang,Xue, Jian,Lin, Xiao-Long,Cai, Tian,Luo, Qun-Li

supporting information, p. 197 - 203 (2020/01/13)

Potassium tert-butoxide-promoted aerobic oxidation of N-alkyl iminium salts is reported. The reaction is atom-economical and environmentally friendly. Iminium salts derived from isoquinoline, quinoline, phenanthridine, phenanthroline, and phthalazine were successfully transformed into their corresponding unsaturated lactams with up to 95% yield under mild conditions in the absence of photocatalysts and metallic or organic catalysts. Owing to the general substrate scope, low cost, feasibility of scale up, wide availability of reagents, and green reaction conditions, this method shows great potential for preparing isoquinolones and related compounds. The method was applied for atom- and step-economical total synthesis of natural products such as norketoyobyrine.

Transfer hydrogenation of isoquinolinium salts catalyzed by a rhodium complex

Wu, Jiashou,Liao, Jian,Zhu, Jin,Deng, Jingen

, p. 2059 - 2062 (2008/02/05)

Regio- and chemoselective transfer hydrogenation of isoquinolinium salts catalyzed by [Cp*RhCl2]2 using HCOOH-Et3N (5:2) as a hydrogen source was realized. A variety of N-methyl- and N-benzyl-1,2,3,4-tetrahydroisoquinoline

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