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Pyridine, 2-[(2,4-dinitrophenyl)methyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25927-45-1

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25927-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25927-45-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,2 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25927-45:
(7*2)+(6*5)+(5*9)+(4*2)+(3*7)+(2*4)+(1*5)=131
131 % 10 = 1
So 25927-45-1 is a valid CAS Registry Number.

25927-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2,4-dinitrophenyl)methyl]-4-methylpyridine

1.2 Other means of identification

Product number -
Other names 2(2,4-dinitrobenzyl)-4-methyl pyridine

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:25927-45-1 SDS

25927-45-1Downstream Products

25927-45-1Relevant academic research and scientific papers

Site selective processes: A combined theoretical and experimental investigation of thermally activated tautomerization processes in 2(2,4-dinitrobenzyl) pyridine derivatives

Khatib,Tal,Godsi,Peskin,Eichen

, p. 6753 - 6761 (2007/10/03)

The thermally activated NH→CH tautomerization process in crystals of 2(2,4-dinitrobenzyl) pyridine derivatives was investigated. The results indicate the absence of any trivial molecular structure-reactivity correlation, in contrast to what is found for similar systems in solutions. The absence of molecular structure-reactivity correlation in the crystalline state is attributed to the participation of neighboring molecules in the proton transfer process. A combined experimental and theoretical approach is presented and applied to the study of the tautomerization reaction in crystalline environments. (C) 2000 Elsevier Science Ltd.

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