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o-(N-allyl-N-methylamino)iodobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57056-87-8

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57056-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57056-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,5 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57056-87:
(7*5)+(6*7)+(5*0)+(4*5)+(3*6)+(2*8)+(1*7)=138
138 % 10 = 8
So 57056-87-8 is a valid CAS Registry Number.

57056-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-allyl-2-iodo-N-methylaniline

1.2 Other means of identification

Product number -
Other names N-allyl-N-methyl-2-iodoaniline

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:57056-87-8 SDS

57056-87-8Relevant academic research and scientific papers

1,3-disubstituted indoline derivative and preparation method thereof

-

Paragraph 0072; 0073; 0074, (2020/02/27)

The invention relates to a 1,3-disubstituted indoline derivative and a preparation method thereof, and belongs to the field of organic compound synthesis. The preparation method comprises following steps: step one, according to a mole ratio of (1-3): (2-1

Radical Hydrodeiodination of Aryl, Alkenyl, Alkynyl, and Alkyl Iodides with an Alcoholate as Organic Chain Reductant through Electron Catalysis

Dewanji, Abhishek,Mück-Lichtenfeld, Christian,Studer, Armido

supporting information, p. 6749 - 6752 (2016/06/09)

A simple and efficient method for radical hydrodeiodination is reported. The novel approach uses electron catalysis. In situ generated Na-alcoholates are introduced as radical chain reducing reagents and reactions work with O2as cheap initiator. Hydrodeiodination works on aryl, alkenyl, alkynyl iodides and a tert-alkyl iodide also gets reduced applying the method. Albeit less general, the method is also applicable to the reduction of aryl bromides. The novel reagent is successfully used to conduct typical reductive radical cyclization reactions and mechanistic studies are reported.

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