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1,1':3',1'':3'',1''':3''',1'''':3'''',1'''''-Sexiphenyl, 2,2',2'',2''',2'''',2'''''-hexafluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88229-85-0

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88229-85-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88229-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,2 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 88229-85:
(7*8)+(6*8)+(5*2)+(4*2)+(3*9)+(2*8)+(1*5)=170
170 % 10 = 0
So 88229-85-0 is a valid CAS Registry Number.

88229-85-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-1-[2-fluoro-3-[2-fluoro-3-[2-fluoro-3-(2-fluorophenyl)phenyl]phenyl]phenyl]-3-(2-fluorophenyl)benzene

1.2 Other means of identification

Product number -
Other names 1,1':3',1'':3'',1''':3''',1'''':3'''',1'''''-Sexiphenyl,2,2',2'',2''',2'''',2'''''-hexafluoro

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:88229-85-0 SDS

88229-85-0Downstream Products

88229-85-0Relevant academic research and scientific papers

Catalyst-Free Synthesis of O-Heteroacenes by Ladderization of Fluorinated Oligophenylenes

Feofanov, Mikhail,Akhmetov, Vladimir,Takayama, Ryo,Amsharov, Konstantin

supporting information, p. 5199 - 5203 (2021/02/21)

A novel catalyst-free approach to benzoannulated oxygen-containing heterocycles from fluorinated oligophenylenes is reported. Unlike existing methods, the presented reaction does not require an oxygen-containing precursor and relies on an external oxygen source, potassium tert-butoxide, which serves as an O2? synthon. The radical nature of the reaction facilitates nucleophilic substitution even in the presence of strong electron-donating groups and enables de-tert-butylation required for the complete annulation. Also demonstrated is the applicability of the method to introduce five-, six-, and seven-membered rings containing oxygen, whereas multiple annulations also open up a short synthetic path to ladder-type O-heteroacenes and oligodibenzofurans.

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