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26482-55-3

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26482-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26482-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,8 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26482-55:
(7*2)+(6*6)+(5*4)+(4*8)+(3*2)+(2*5)+(1*5)=123
123 % 10 = 3
So 26482-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N3O2/c9-8(10)7-5-1-3-6-4-2-5/h1-4H,(H,6,7)(H,9,10)/q+1

26482-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-pyridin-4-ylnitramide

1.2 Other means of identification

Product number -
Other names 4-Nitroaminopyridine

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:26482-55-3 SDS

26482-55-3Upstream product

26482-55-3Relevant articles and documents

Preparation of novel 2,3,8-trisubstituted pyrido[3,4-b]pyrazines and pyrido[2,3-b]pyrazines

Antoine, Maud,Czech, Michael,Gerlach, Matthias,Guenther, Eckhard,Schuster, Tilmann,Marchand, Pascal

experimental part, p. 794 - 806 (2011/04/16)

A four-step synthesis of 8-bromo-2,3-disubstituted pyrido[3,4-b]pyrazines and a six-step synthesis of 8-amino-2,3-disubstituted pyrido[3,4-b]pyrazines have been developed. A particularly valuable feature of this synthetic route is the possibility to build

Substituent Effects on the Isomer Ratios in the Rearrangement of Some 2- and 4-Nitraminopyridines

Deady, Leslie W.,Korytsky, Olga L.,Rowe, Jeffrey E.

, p. 2025 - 2034 (2007/10/02)

The preparation, and rearrangement in 92percent sulfuric acid, of 4-X-2-nitramino- (1), 2-X-4-nitramino- (2), and 6-X-2-nitramino-pyridines (3) is reported (X=H,Me,MeO,Br,Cl,CO2H).The product isomer ratios can be explained by differential electronic stabilization of the appropriate ? complexes for aromatic nitration and steric effects seem relatively unimportant.Deuteration had no effect on the product distribution

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