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1-Chloro-1,1-dinitroethane is an organic compound with the chemical formula C2H2ClN2O4. It is a colorless, oily liquid that is highly sensitive to shock and friction, making it a potential explosive. 1-Chloro-1,1-dinitroethane is characterized by the presence of a chloro group (-Cl), two nitro groups (-NO2), and an ethyl group (-CH2CH3). It is synthesized by reacting 1,1-dinitroethane with chlorine in the presence of a catalyst. Due to its hazardous nature, 1-chloro-1,1-dinitroethane is primarily used in research and development for the production of explosives and propellants. It is important to handle this chemical with extreme caution, as it can decompose upon heating or exposure to flame, releasing toxic fumes and potentially causing a violent explosion.

2972-95-4

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2972-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2972-95-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2972-95:
(6*2)+(5*9)+(4*7)+(3*2)+(2*9)+(1*5)=114
114 % 10 = 4
So 2972-95-4 is a valid CAS Registry Number.
InChI:InChI=1/C2H3ClN2O4/c1-2(3,4(6)7)5(8)9/h1H3

2972-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1,1-dinitroethane

1.2 Other means of identification

Product number -
Other names ETHANE,1-CHLORO-1,1-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:2972-95-4 SDS

2972-95-4Downstream Products

2972-95-4Relevant academic research and scientific papers

REACTION OF DINITROMETHYL COMPOUNDS WITH XENON DIFLUORIDE IN VARIOUS SOLVENTS

Tselinskii, I. V.,Mel'nikov, A. A.,Trubitsin, A. E.

, p. 1485 - 1487 (2007/10/02)

The products from the reaction of xenon difluoride with the potassium salts of a series of dinitromethyl compounds ( dinitromethane, trinitromethane, 1,1-dinitroethane, phenyldinitromethane) in methylene chloride, carbon tetrachloride, and acetonitrile were investigated.On the basis of the data from analysis by GLC and UV spectroscopy it was found that in most cases the reaction takes place with the participation of solvent molecules.The proposed reaction mechanism includes a stage of one-electron oxidation of the anion of the dinitromethyl compound by the XeF2 molecule to a dinitromethyl radical.

REACTION OF 1,1-DINITROETHANE POTASSIUM SALT WITH XENON DIFLUORIDE

Tselinskii, I. V.,Mel'nikov, A. A.,Varyagina, L. G.,Trubitsin, A. E.

, p. 2276 - 2279 (2007/10/02)

The potassium salt of 1,1-dinitroethane reacts with xenon difluoride in methylene chloride to form a mixture of products, i.e., acetic acid, 1-fluoro-1,1-dinitroethane, 1-chloro-1,1-dinitroethane, 1,1,1-trinitroethane, and 1,1-dinitroethane.The ratios of the yields depend on the reaction conditions.The proposed mechanism for the formation of the reaction products involves one-electron oxidation of the dinitroethane radical, which enters into reaction with the methylene chloride molecules and intermediate radical particles.

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