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2H-Isoindole, 4,5,6,7-tetrafluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55164-85-7

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55164-85-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55164-85-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,6 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55164-85:
(7*5)+(6*5)+(5*1)+(4*6)+(3*4)+(2*8)+(1*5)=127
127 % 10 = 7
So 55164-85-7 is a valid CAS Registry Number.

55164-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5,6,7-tetrafluoro-2H-isoindole

1.2 Other means of identification

Product number -
Other names 2H-Isoindole,4,5,6,7-tetrafluoro

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:55164-85-7 SDS

55164-85-7Upstream product

55164-85-7Relevant academic research and scientific papers

The polymer and diarylisoindoles

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Paragraph 0111 - 0114, (2016/10/09)

PROBLEM TO BE SOLVED: To provide a novel method for easily producing an isoindole. SOLUTION: The method for producing an isoindole represented by formula (2) is characterized by reducing a phthalonitrile represented by formula (1). In the formulae,

Novel preparation of fluorinated isoindoles and their conversion to fluorinated benzoporphyrins

Uno, Hidemitsu,Masuda, Go,Tukiji, Marie,Nishioka, Yuiko,Iida, Toshiya

, p. 7512 - 7515 (2008/03/14)

4,5,6,7-Tetrafluoroisoindole and their related compounds were prepared directly from the corresponding phthalonitriles by reduction of a hydride reagent such as DIBAL or catalytic hydrogenation in the presence of an acid. 4,5,6,7-Tetrafluoroisoindole was

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