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Dinitrofluoromethane, also known as 1,1-dinitro-1-fluoromethane or fluorodinitromethane, is a chemical compound with the formula C(F)(NO2)2. It is a colorless, oily liquid that is highly toxic and explosive. Dinitrofluoromethane is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Dinitrofluoromethane is produced by the reaction of fluoromethane with nitric acid and is used as a reagent in the preparation of various fluorinated compounds. Due to its hazardous nature, it requires careful handling and storage to prevent accidents.

7182-87-8

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7182-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7182-87-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,8 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7182-87:
(6*7)+(5*1)+(4*8)+(3*2)+(2*8)+(1*7)=108
108 % 10 = 8
So 7182-87-8 is a valid CAS Registry Number.
InChI:InChI=1/CHFN2O4/c2-1(3(5)6)4(7)8/h1H

7182-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name fluoro(dinitro)methane

1.2 Other means of identification

Product number -
Other names Dinitrofluoromethane

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:7182-87-8 SDS

7182-87-8Relevant academic research and scientific papers

CHEMICAL GENERATION OF TRINITROMETHYL RADICALS IN THE REACTION OF XENON DIFLUORIDE WITH THE NITROFORM ANION

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

, p. 619 - 622 (2007/10/02)

In the reaction between the trinitromethane potassium salt and xenon difluoride in acetonitrile in the presence of benzene and THF the trinitromethyl derivatives of benzene and THF are formed in addition to the fluorination products.This indicates that the reaction takes place through the formation of trinitromethyl radicals.

Pressure-Induced Cyclotrimerization of Electron-Deficient Nitriles. Catalysis by Acidic Alcohols and Phenols

Koppes, William M.,Adolph, Horst G.

, p. 406 - 412 (2007/10/02)

Fluorodinitroacetonitrile (1) was pressurized at 1 GPa in the presence of a variety of ROH catalysts.Cyclotrimerization of 1 occurred in several cases, but the observed triazines contained RO groups in place of one or several CF(NO2)2 groups.Some mechanistic aspects of this reaction are explored by comparison with the results of the pressurization of preformed fluorodinitroacetimidates.

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