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Benzenamine, N-(2-quinoxalinylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104182-63-0

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104182-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104182-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104182-63:
(8*1)+(7*0)+(6*4)+(5*1)+(4*8)+(3*2)+(2*6)+(1*3)=90
90 % 10 = 0
So 104182-63-0 is a valid CAS Registry Number.

104182-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenyl-1-quinoxalin-2-ylmethanimine

1.2 Other means of identification

Product number -
Other names Chinoxalin-2-ylmethylen-anilin

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:104182-63-0 SDS

104182-63-0Relevant academic research and scientific papers

Diels-Alder Reactions with Ethylene and Superelectrophiles

Vuong, Hien,Dash, Barada P.,Nilsson Lill, Sten O.,Klumpp, Douglas A.

, p. 1849 - 1852 (2018)

Diels-Alder reactions have been accomplished with ethylene as the dienophile through the use of inverse-electron demand Diels-Alder chemistry. As a key aspect of the chemistry, the dienes are part of tri- or dicationic superelectrophilic systems. Theoreti

Superelectrophilic Diels–Alder reactions and oxidations leading to heterocyclic biaryl compounds

Vuong, Hien,Klumpp, Douglas A.

, p. 316 - 323 (2019)

Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation involves a Diels–Alder reaction with a multiply protonated imine to give a tetrahydroquinoline product, whereas the second step involves oxidation with elem

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