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1,2-Dinitroethane, with the molecular formula C2H4N2O4, is a colorless, oily liquid characterized by a faint, sweet odor. It is recognized for its volatility and flammability, which can lead to the production of toxic gases upon combustion. Due to its potential hazards, it requires careful handling and storage to ensure safety and prevent harm to human health and the environment.

7570-26-5

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7570-26-5 Usage

Uses

Used in Explosive Synthesis:
1,2-Dinitroethane is used as a stabilizer in the synthesis of explosives, contributing to the stability and performance of the final explosive products.
Used in Chemical Reactions:
1,2-Dinitroethane serves as a solvent in certain chemical reactions, facilitating the process and aiding in the achievement of desired outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 7570-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7570-26:
(6*7)+(5*5)+(4*7)+(3*0)+(2*2)+(1*6)=105
105 % 10 = 5
So 7570-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H4N2O4/c5-3(6)1-2-4(7)8/h1-2H2

7570-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dinitroethane

1.2 Other means of identification

Product number -
Other names Ethane, 1,2-dinitro-

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:7570-26-5 SDS

7570-26-5Relevant academic research and scientific papers

Polyfunctional pyridines from nitroacetamidine and β-diketones. A useful synthesis of substituted imidazo[4,5-b]pyridines and related compounds

Batt,Houghton

, p. 963 - 969 (2007/10/02)

Nitroacetamidine undergoes a useful cyclocondensation with β-diketones to produce substituted 2-amino-3-nitropyridines. Use of an acylpyruvate generates hitherto unreported 2-amino-3-nitropyridine-4-carboxylates. These may be converted easily to functionalized imidazo[4,5-b]pyridines and oxazolo[5,4-b]pyridines.

ELECTRON SPIN RESONANCE STUDIES. PART 64. THE HYDROXYL RADICAL-INDUCED DECARBOXYLATION OF METHIONINE AND SOME RELATED COMPOUNDS

Davies, Michael J.,Gilbert, Bruce C.,Norman, Richard O.

, p. 731 - 738 (2007/10/02)

Spin-trapping e.s.r. experiments employing both MeNO2 (in conjunction with generation of .OH from the TiIII-H2O2 couple in a flow system) and ButNO ( in conjunction with the photolytic decomposition of H2O2) confirm that the reaction of .OH with methionine, S-methylcysteine, and some related compounds effects oxidative decarboxylation.It is proposed that the reaction proceeds via the sequential formation of an hydroxyl adduct at sulphur, a sulphur-centred radical-cation, and a (cyclic) sulphuranyl radical in which the carboxylate function becomes bonded to sulphur.

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