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1,1'-Biphenyl, 2,2',3,3',4,5,5',6,6'-nonafluoro-4'-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5121-76-6

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5121-76-6 Usage

Type of Compound

Perfluorinated compound

Applications

Production of electronic materials (e.g., polymers and liquid crystals)
Solvent for certain reactions
Reagent in organic synthesis

Chemical Properties

Unique chemical properties
High thermal stability

Environmental Impact

Considered a persistent organic pollutant
Potential environmental impact and toxicity concerns

Management

Careful use and disposal to minimize adverse effects on the environment and human health

Check Digit Verification of cas no

The CAS Registry Mumber 5121-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,2 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5121-76:
(6*5)+(5*1)+(4*2)+(3*1)+(2*7)+(1*6)=66
66 % 10 = 6
So 5121-76-6 is a valid CAS Registry Number.

5121-76-6SDS

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 1,2,3,4,5-pentafluoro-6-[2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl]benzene

1.2 Other means of identification

Product number -
Other names Nonafluor-4-trifluormethyl-diphenyl

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:5121-76-6 SDS

5121-76-6Downstream Products

5121-76-6Relevant academic research and scientific papers

Formation of perfluorinated polyphenylenes by multiple pentafluorophenylation using C6F5Si(CH3) 3

Nishida, Masakazu,Hayakawa, Yoshio,Ono, Taizo

experimental part, p. 1314 - 1321 (2011/02/22)

Pentafluorophenylation of perfluoroarenes with C6F 5Si(CH3)3 was investigated by using NMR and MALDI-TOF-MS techniques. Successive multiple pentafluorophenylation easily occurred not only on the para-position but also on the ortho-positions to provide perfluorinated p-phenylene and m-phenylene compounds. The perfluoroarenes having electron-withdrawing substituents provided oligo- to poly-(phenylene)s depending on the added amounts of C6F 5Si(CH3)3, while the perfluoroarenes having electron-donor substituents gave H(C6F4)nF polymers produced from C6F5H, which was the decomposed product of C6F5Si(CH3)3.

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