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2,3-Pyridinedicarboxamide, N,N'-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94301-63-0

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94301-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94301-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 94301-63:
(7*9)+(6*4)+(5*3)+(4*0)+(3*1)+(2*6)+(1*3)=120
120 % 10 = 0
So 94301-63-0 is a valid CAS Registry Number.

94301-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name quinolinic acid dianilide

1.2 Other means of identification

Product number -
Other names pyridine-2,3-dicarboxylic acid-dianilide

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:94301-63-0 SDS

94301-63-0Relevant academic research and scientific papers

Palladium-catalysed aminocarbonylation of diiodopyridines

Takács, Attila,Varga, Georgina Márta,Kardos, Johanna,Kollár, László

, p. 2131 - 2138 (2017/03/17)

The aminocarbonylation of 2,5- and 2,3-diiodopyridine, as well as 2-chloro-3,4-diiodopyridine with carbon monoxide and various primary and secondary amines was carried out using palladium-catalysed aminocarbonylation. The formation of the products contain

Improved synthesis of N-substituted 2,3-pyridine-dicarboximides with microwave irradiation

Blanco, Maria M.,Levin, Gustavo J.,Schapira, Celia B.,Perillo, Isabel A.

, p. 1881 - 1890 (2007/10/03)

The microwave-induced synthesis of N-substituted 2,3- pyridinedicarboximides (1) by means of two different approaches is presented. One involves direct N-alkylation of quinolinimide (2) (Method A) and the other, dehydrative condensation of quinolinic anhydride (4) and amines (Method B). Reactions resulted highly accelerated, with improved yields in relation to those obtained by conventional heating. The scope and limitations of each method and its variants are discussed.

New synthesis of pyrido[2,3-d] and [3,2-d]oxazines

Fahmy, Amin F.,Sauer, Juergen,Youssef, Mohamed Salah K.,Halim, Mohamed Said Abdel,Hassan, Mamdouh A.

, p. 2871 - 2886 (2007/10/03)

N-Hydroxyquinolinimide 1 reacts with each of aromatic arnines, hydrazine hydrate and aromatic hydrocarbons to give arylcarbamoyl pyridines 2, pyrrolopyridines 3, pyridopyridazines 4 and pyridooxazinones 5 and 6. The heterocycles 5 and 6 can be transformed

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