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Methyldifluoroarsine, also known as CH3AsF2, is a colorless, toxic gas with a pungent odor. It is an organoarsenic compound consisting of one carbon atom, one hydrogen atom, and two fluorine atoms bonded to a central arsenic atom. Methyldifluoroarsine is a derivative of arsine (AsH3), where one hydrogen atom is replaced by a methyl group (CH3). Methyldifluoroarsine is highly reactive and can be used as a precursor in the synthesis of various organoarsenic compounds. Due to its toxicity and potential environmental impact, it is essential to handle methyldifluoroarsine with extreme caution and in accordance with proper safety protocols.

420-24-6

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420-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 420-24-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,2 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 420-24:
(5*4)+(4*2)+(3*0)+(2*2)+(1*4)=36
36 % 10 = 6
So 420-24-6 is a valid CAS Registry Number.
InChI:InChI=1/CH3AsF2/c1-2(3)4/h1H3

420-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name difluoro(methyl)arsane

1.2 Other means of identification

Product number -
Other names Methylarsonous difluoride

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:420-24-6 SDS

420-24-6Downstream Products

420-24-6Relevant academic research and scientific papers

Synthesis and biological screening of trifluoromethylthioarsenicals

Munavalli, S.,Rossman, D. I.,Rohrbaugh, D. K.,Ferguson, C. P.,Buettner, L.

, p. 15 - 20 (2007/10/02)

The title compounds have been prepared from the reaction of trifluoromethylthiocopper and alkyl mono- and di-haloarsines.This communication describes their synthesis, biological screening and mass spectral fragmentation behavior.

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