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Benzenamine, N,N'-1,2-ethanediylidenebis[4-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70735-06-7

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70735-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70735-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,3 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70735-06:
(7*7)+(6*0)+(5*7)+(4*3)+(3*5)+(2*0)+(1*6)=117
117 % 10 = 7
So 70735-06-7 is a valid CAS Registry Number.

70735-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(4-fluorophenyl)ethane-1,2-diimine

1.2 Other means of identification

Product number -
Other names 1,4-bis(4-fluorolphenyl)-1,4-diaza-1,3-butadiene

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:70735-06-7 SDS

70735-06-7Relevant academic research and scientific papers

Cationic rhodium(I) and iridium(I) α-diimine complexes

Harding, Duncan A.J.,Hope, Eric G.,Singh, Kuldip,Solan, Gregory A.

experimental part, p. 360 - 366 (2012/03/12)

Condensation of glyoxal with fluoroarylanilines [ArFNH 2; ArF = 4-C6H4F; 2,4-C 6H3F2; 2,4,6-C6H2F 3] generates new fluorine-substitute

A greener method towards the synthesis of 1,3-diarylimidazolium tetrafluoroborates

Ikhile, Monisola I.,Bala, Muhammad D.,Nyamori, Vincent O.

experimental part, p. 101 - 104 (2012/07/03)

A new strategic method for the synthesis of 1,3-diarylimidazolium tetrafluoroborate salts is illustrated herein. A solvent-free approach was employed in the synthesis of thediimines which are precursors in the preparation of the imidazolium salts. The reaction proceeds faster, cleaner and in a better yield than previously reported methods.

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