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2-Octanol, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89807-96-5

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89807-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89807-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89807-96:
(7*8)+(6*9)+(5*8)+(4*0)+(3*7)+(2*9)+(1*6)=195
195 % 10 = 5
So 89807-96-5 is a valid CAS Registry Number.

89807-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-phenylsulfanyloctan-2-ol

1.2 Other means of identification

Product number -
Other names trihydryl-1,1,2 phenylthio-1 F-octanol-2

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:89807-96-5 SDS

89807-96-5Relevant academic research and scientific papers

REACTION D'OUVERTURE DES F-ALKYL OXIRANNES

Coudures, C.,Pastor, R.,Szonyi, S.,Cambon, A.

, p. 105 - 116 (1984)

Reactivity of F-alkyl oxirans was investigated towards nucleophilic and electrophilic reagents.They are quite inert in acid medium.On the other hand, in basic medium they lead to regiospecific opening reactions.Their reactions with organometallic compound

Synthesis and Pummerer reaction of 2-F-alkyl-2-hydroxyethylphenyl sulfoxides

Hedhli, Ahmed,Szoenyi, Stephane,Baklouti, Ahmed,Cambon, Aime

, p. 133 - 138 (2007/10/02)

The synthesis of new 2-F-alkyl-2-hydroxyethylphenyl sulfoxides 3 and their 2-methyl ethers 4 is reported.They undergo the Pummerer rearrangement to yield 2-F-alkyl-1,2-diacetoxyethylphenyl sulfides 7 and 2-F-alkyl-1-acetoxy-2-methoxyethylphenyl sulfides 8

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