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Fluoroacetic anhydride, with the chemical formula C2H2F2O3, is a colorless and pungent-smelling liquid that exhibits high reactivity. This characteristic makes it a valuable compound in various chemical reactions, particularly in the synthesis of organic compounds. However, its reactivity also necessitates careful handling and storage to prevent severe burns upon skin contact and other potential hazards.

407-33-0

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407-33-0 Usage

Uses

Used in Pharmaceutical Industry:
Fluoroacetic anhydride is utilized as a key reagent in the synthesis of pharmaceuticals. Its high reactivity allows for the efficient production of various drug compounds, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, fluoroacetic anhydride serves as an essential component in the creation of pesticides and other crop protection agents. Its role in these syntheses helps to ensure the production of effective and targeted agrochemicals for agricultural use.
Used as a Research Reagent:
Fluoroacetic anhydride is also employed as a research reagent in various scientific studies and experiments. Its unique properties and reactivity make it a valuable tool for exploring new chemical reactions and developing innovative synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 407-33-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 407-33:
(5*4)+(4*0)+(3*7)+(2*3)+(1*3)=50
50 % 10 = 0
So 407-33-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H4F2O3/c5-1-3(7)9-4(8)2-6/h1-2H2

407-33-0SDS

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 (2-fluoroacetyl) 2-fluoroacetate

1.2 Other means of identification

Product number -
Other names 2-fluoroacetic anhydride

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:407-33-0 SDS

407-33-0Relevant academic research and scientific papers

PYRAZOLO-PYRROLIDIN-4-ONE DERIVATIVES AS BET INHIBITORS AND THEIR USE IN THE TREATMENT OF DISEASE

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Page/Page column 49, (2014/12/12)

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; (l) a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

IMIDAZOPYRROLIDINONE DERIVATIVES AND THEIR USE IN THE TREATMENT OF DISEASE

-

Page/Page column 155, (2014/12/12)

The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof; a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

Efficient and convenient synthesis of symmetrical carboxylic anhydrides from carboxylic acids with sulfated zirconia by phase transfer catalysis

Hu, Yu Lin,Zhao, Xing E.,Lu, Ming

experimental part, p. 255 - 262 (2012/04/17)

An efficient and convenient procedure for the synthesis of symmetrical carboxylic anhydrides from carboxylic acids with sulfated zirconia by PEG-1000 phase transfer catalysis has been developed. The reactions proceeded under mild and solvent-free conditions to provide the carboxylic anhydrides in good to excellent yields. The product can be isolated by a simple extraction with organic solvent, and the catalyst system can be recycled or reused without any significant loss of catalytic activity.

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