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2-Pyridinamine,N-methyl-3,5-dinitro-(9CI) is a chemical compound with the molecular formula C7H7N5O4. It is a derivative of pyridinamine, featuring a methyl group and two nitro groups attached to its structure. 2-Pyridinamine,N-methyl-3,5-dinitro-(9CI) is known for its potential applications in the agricultural sector, particularly as a pesticide and herbicide.

19404-40-1

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19404-40-1 Usage

Uses

Used in Agricultural Industry:
2-Pyridinamine,N-methyl-3,5-dinitro-(9CI) is used as a pesticide for controlling pests and as a herbicide for managing weeds in various crops. Its application helps protect plants from damage caused by insects and unwanted vegetation, thereby ensuring healthier and more productive crops.
However, it is crucial to handle 2-Pyridinamine,N-methyl-3,5-dinitro-(9CI) with care, as it may pose risks to human health and the environment due to its potential toxicity. Further research and the implementation of safety measures are essential to mitigate any adverse effects and to fully understand the benefits and drawbacks of using 2-Pyridinamine,N-methyl-3,5-dinitro-(9CI) in agriculture.

Check Digit Verification of cas no

The CAS Registry Mumber 19404-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19404-40:
(7*1)+(6*9)+(5*4)+(4*0)+(3*4)+(2*4)+(1*0)=101
101 % 10 = 1
So 19404-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4O4/c7-2-5-6(10(13)14)1-4(3-8-5)9(11)12/h1,3H,2,7H2

19404-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-3,5-dinitropyridin-2-amine

1.2 Other means of identification

Product number -
Other names (3,5-Dinitro-[2]pyridyl)-methyl-amin

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:19404-40-1 SDS

19404-40-1Relevant academic research and scientific papers

INHIBITORS OF NECROPTOSIS

-

Page/Page column 27; 28, (2021/09/04)

This invention relates to compounds of Formula (I) and salts, solvates, prodrugs, tautomers, N-oxides, stereoisomers, polymorphs and physiologically functional derivatives thereof. Also disclosed are methods of use of Formula (I), including in the inhibition of necroptosis and treatment of associated diseases, conditions and/or disorders.

Nitration of Some Derivatives of 2- Methylaminopyridine N-Oxides

Talik, Tadeusz,Talic, Zofia

, p. 84 - 88 (2007/10/02)

The only stable products obtained from nitrations of 2-methylaminopyridine N-oxide and some derivatives, are those resulting from nitration of the pyridine ring.Thus, 2-methyl-aminopyridine N-oxide 8 is nitrated under mild conditions to yield 2-methylamino-5-nitropyridine N-oxide 9, but not 2-methylnitraminopyridine-N-oxide as might be expected.Under stronger nitrating conditions 2-methylamino-3,5-dinitropyridine N-oxide 10 is obtained. 2-Methylamino-4-nitropyridine N-oxide 1 yields 2-methylamino-4,5-dinitropyridine N-oxide 2 upon nitration.Chemical reactions which re late known compounds to the new compounds obtained, confirm the assigned structures.

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