Welcome to LookChem.com Sign In|Join Free
  • or
Tetrafluorosuccinamide is a fluoride compound frequently used in chemical research. It is characterized by its molecular weight, melting point, boiling point, and chemical formula, which make it essential for specific chemical reactions, especially in organic synthesis. Due to the potential for hazardous reactions, it is crucial to exercise caution when handling this chemical. Ongoing studies are being conducted to further explore its various potential applications.

377-37-7

Post Buying Request

377-37-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

377-37-7 Usage

Uses

Used in Chemical Research:
Tetrafluorosuccinamide is used as a chemical compound for facilitating specific chemical reactions. Its unique properties, such as molecular weight and melting point, make it a valuable component in the field of chemical research.
Used in Organic Synthesis:
In the realm of organic synthesis, Tetrafluorosuccinamide is employed as a reagent to aid in the formation of complex organic molecules. Its role in these reactions is crucial for the development of new compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 377-37-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 377-37:
(5*3)+(4*7)+(3*7)+(2*3)+(1*7)=77
77 % 10 = 7
So 377-37-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H4F4N2O2/c5-3(6,1(9)11)4(7,8)2(10)12/h(H2,9,11)(H2,10,12)

377-37-7SDS

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 Tetrafluorosuccinamide

1.2 Other means of identification

Product number -
Other names TETRAFLUOROSUCCINAMIDE

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:377-37-7 SDS

377-37-7Relevant academic research and scientific papers

Octafluoro-meso-tetraarylporphyrins and methods for making these compounds

-

, (2008/06/13)

The novel compounds of the present invention are beta -octafluoro-meso-tetraarylporphyrins of formula (I) and their metallic complexes of formula (II): beta -octafluoro-meso-tetraaryl porphyrins are synthesized by reacting 3,4-difluoropyrrole with an aromatic aldehyde in the presence of boron trifluoride etherate, followed by oxidation. The difluoropyrrole used in this reaction is produced by reacting 3,3,4,4-tetrafluoropyrroline or its corresponding salt, 3,3,4,4-tetrafluoropyrrolidinium salt, with a base such as potassium tert-butoxide. The metalloporphyrins of the present invention are synthesized by deprontonating beta -octafluoro-meso-tetraarylporphyrin ligands and treating said ligands with metal ions.

Use of Perfluoroalkylfluorosulfonates for Synthesizing Organofluorine Compounds

Rapkin, A. I.,Zabolot-skikh, V. F.,Kochanov, A. S.,Tiunov, A. V.,Zhirnov, O. M.

, p. 133 - 134 (2007/10/03)

The possibility of using fluorosulfation for synthesizing perfluorovinyl and perfluorodivinyl ethers, and also perfluorocarboxylic and perfluorodicarboxylic acids, has been studied.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 377-37-7