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Acetyl fluoride, chlorooxo-, also known as chlorooxirane-acetic acid fluoride, is a chemical compound with the formula C3H3ClO2F. It is a colorless liquid that is soluble in water and has a pungent odor. Acetyl fluoride, chlorooxo- is primarily used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It is also employed as a fluorinating agent in various chemical reactions. Due to its reactivity and potential hazards, it is important to handle acetyl fluoride, chlorooxo- with proper safety measures and in accordance with established guidelines.

431-10-7

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431-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 431-10-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 431-10:
(5*4)+(4*3)+(3*1)+(2*1)+(1*0)=37
37 % 10 = 7
So 431-10-7 is a valid CAS Registry Number.

431-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-2-oxoacetyl fluoride

1.2 Other means of identification

Product number -
Other names oxalyl chlorofluoride

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:431-10-7 SDS

431-10-7Upstream product

431-10-7Downstream Products

431-10-7Relevant academic research and scientific papers

Fluorinated olefins and oleum

Cheburkov, Yuri,Lamanna, William M.

, p. 147 - 152 (2003)

Oleum has some advantages over pure sulfur trioxide and may be successfully used for preparation of beta-sultones from hexafluoropropene, 2H-pentafluoropropene, 6H-perfluoro-1-hexene and perfluoro(propylvinyl) ether (VE). Depending on the reaction conditi

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