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89807-87-4

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89807-87-4 Usage

General Description

(NONAFLUORO-N-BUTYL)EPOXIDE is a fluorinated compound that belongs to the group of epoxides, which are organic compounds containing a three-membered ring consisting of an oxygen atom and two carbon atoms. This particular chemical is formed by replacing the hydrogen atoms in the butyl group of n-butyl vinyl ether with nonafluoro groups, resulting in a highly fluorinated compound. It is often used as a building block for the synthesis of various fluorinated compounds and polymers. Due to its unique fluorinated structure, (NONAFLUORO-N-BUTYL)EPOXIDE has properties that make it useful in applications such as surfactants, lubricants, and inorganic coatings, where its fluorinated nature provides unique surface properties and resistance to chemical and environmental degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 89807-87-4 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, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89807-87:
(7*8)+(6*9)+(5*8)+(4*0)+(3*7)+(2*8)+(1*7)=194
194 % 10 = 4
So 89807-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F9O/c7-3(8,2-1-16-2)4(9,10)5(11,12)6(13,14)15/h2H,1H2

89807-87-4SDS

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 2-(1,1,2,2,3,3,4,4,4-nonafluorobutyl)oxirane

1.2 Other means of identification

Product number -
Other names Nonafluorobutylepoxide

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:89807-87-4 SDS

89807-87-4Relevant articles and documents

NOUVELLES METHODES DE PREPARATION DES F-ALKYL OXIRANES A PARTIR DES ACETATES DE BROMO-2 F-ALKYL-2 ETHYLE ET DES BROMO-2 F-ALKYL-2 ETHANOL

Chaabouni, Mm.,Baklouti, A.,Szonyi, S.,Cambon, A.

, p. 307 - 315 (1990)

F-alkyl oxiranes provide many interesting intermediates.Their synthesis from 2-bromo-2-F-alkylethyl acetates and from 2-bromo-2-F-alkylethanols was improved by two different methods which are very easy to apply.One requires the use of concentrated caustic soda and a phase transfer catalyst; the other one, potassium fluoride in triethylene glycol.

Nouveaux amphiphiles cationiques perfluoroalkyles derives des 1-monotosylate et 1-monobromoacetate de 2-F-alkyl 2-bromo ethanols. II

Nasreddine, M.,Szoenyi, S.,Cambon, A.

, p. 293 - 300 (2007/10/02)

Tosylation, esterification and etherification reactions have been investigated for 2-F-alkyl-2-bromo-ethanols.Intermediates containing a tosyl group or a bromine atom could be converted into corresponding F-alkylated cationic amphiphiles by means of secon

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