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103698-09-5

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103698-09-5 Usage

General Description

4-Pyridinecarbonitrile,3-nitro-(9CI) is a chemical compound with the molecular formula C6H3N3O2. It is a nitro derivative of pyridinecarbonitrile and is commonly used as a building block in organic synthesis. 4-Pyridinecarbonitrile,3-nitro-(9CI) is a pale yellow solid with a slightly bitter taste and is insoluble in water. It is primarily used in the production of pharmaceuticals, agrochemicals, and other organic compounds. 4-Pyridinecarbonitrile,3-nitro-(9CI) has potential applications in the development of new drugs and pesticides due to its unique chemical structure and reactivity. However, it is important to handle this compound with caution as it may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 103698-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,9 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103698-09:
(8*1)+(7*0)+(6*3)+(5*6)+(4*9)+(3*8)+(2*0)+(1*9)=125
125 % 10 = 5
So 103698-09-5 is a valid CAS Registry Number.

103698-09-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitropyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-pyridinecarbonitrile,3-nitro

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:103698-09-5 SDS

103698-09-5Upstream product

103698-09-5Downstream Products

103698-09-5Relevant articles and documents

The synthesis of β-nitropyridine compounds

Bakke, Jan M.,Ranes, Eli,Riha, Jaroslav,Svensen, Harald

, p. 141 - 144 (2007/10/03)

Pyridine and a number of substituted pyridines have been nitrated by reaction with N2O5 followed by reaction with an aqueous solution of SO2xH2O or NaHSO3. The dependence of the yields on the pH of the aqueous reaction medium, on the concentration of SO2xH2O-HSO3-, on addition of methanol to the aqueous phase, and on the reaction temperature were investigated. The yields obtained with NaHSO3 were: 3-nitropyridine 77%, 2-methyl-5-nitro-pyridine 36%, 3-methyl-5-nitropyridinc 24%, 3-acetyl-5-nitropyridine 18%, 5-nitropyridine-3-carboxylic acid 15%, 3-chloro-5-nitropyridine 11%, 4-methyl-3-nitropyridine 39%, 4-acetyl-3-nitropyridine 67%, 4-cyano-3-nitropyridine 45%, 4-phenyl-3-nitropyridine 68%, 4-formyl-3-nitropyridine 62% (from reaction in liquid SO2), 3-nitropyridine-4-carboxylic acid 48%, methyl 3-nitropyridine-4-carboxylate 75%, 2,3-dimethyl-5-nitropyridine 37%, 2,4-dimethyl-5-nitropyridine 64%, 3-nitroquinoline 10% and 4-nitroisoquinoline 42%.

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