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377-37-7

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377-37-7 Usage

General Description

Tetrafluorosuccinamide is a type of fluoride compound often utilized in the field of chemical research. This chemical's properties, which include its molecular weight, melting point, boiling point, and chemical formula, make it integral to specific chemical reactions, particularly those involving organic synthesis. As with other chemicals, necessary precautions should be taken while using it due to the possibility of hazardous reactions. Despite the substantial information about its structure and properties currently known, detailed studies further scrutinizing its various potential applications are continuously ongoing.

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 articles and documents

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.

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