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1-Nonen-3-one, 4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-phenyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89176-08-9

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89176-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89176-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,7 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89176-08:
(7*8)+(6*9)+(5*1)+(4*7)+(3*6)+(2*0)+(1*8)=169
169 % 10 = 9
So 89176-08-9 is a valid CAS Registry Number.

89176-08-9SDS

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 4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-phenylnon-1-en-3-one

1.2 Other means of identification

Product number -
Other names 1-Nonen-3-one,4,4,5,5,6,6,7,7,8,8,9,9,9-tridecafluoro-1-phenyl-,(E)

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:89176-08-9 SDS

89176-08-9Downstream Products

89176-08-9Relevant academic research and scientific papers

Preparation of Perfluoroalkyl Ketones by the Reaction of Perfluoroalkyllithiums with Esters

Uno, Hidemitsu,Shiraishi, Yasukazu,Suzuki, Hitomi

, p. 2636 - 2642 (2007/10/02)

A variety of esters react with perfluoroalkyllithiums in situ generated from perfluoroalkyl iodides and methyllithium to give perfluoroalkyl ketones in good yields.Perfluoroalkyllithiums add to α,β-unsaturated esters only in the 1,2-addition mode even in the presence of copper salt.Exception was observed in the reaction with maleates where perfluoroalkylated succinic esters and normal 1,2-addition products are obtained in comparable amounts.

An Efficient Synthesis of Perfluoroalkyl Ketones Using Perfluoroalkyllithiums

Uno, Hidemitsu,Shiraishi, Yasukazu,Simokawa, Kazuhiro,Suzuki, Hitomi

, p. 1153 - 1156 (2007/10/02)

Perfluoroalkylation of esters with perfluoroalkyllithiums occurs smoothly in ether at -78 deg C, giving the corresponding perfluoroalkyl ketones in good yields.

NOVEL SYNTHESIS OF F-1-ALKENE-1-PHOSPHONATE DERIVATIVES FROM F-ALKANOYL CHLORIDES AND THEIR EFFICIENT USE FOR PREPARING FLUORO-α,β-ENONES

Ishihara, Takashi,Maekawa, Takashige,Ando, Teiichi

, p. 4229 - 4232 (2007/10/02)

(Z)-1--F-1-alkene-1-phosphonates were synthesized in good yields from F-alkanoyl chlorides and triethyl phosphite, and were proved to be useful precursors for the preparation of fluoro-α,β-enones.

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