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86714-24-1

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86714-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86714-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,1 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86714-24:
(7*8)+(6*6)+(5*7)+(4*1)+(3*4)+(2*2)+(1*4)=151
151 % 10 = 1
So 86714-24-1 is a valid CAS Registry Number.

86714-24-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name F-3-propoxy-2-methylpentane

1.2 Other means of identification

Product number -
Other names 1,1,1,2,2,3,4,5,5,5-Decafluoro-3-heptafluoropropyloxy-4-trifluoromethyl-pentane

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:86714-24-1 SDS

86714-24-1Downstream Products

86714-24-1Relevant articles and documents

A NEW SYNTHETIC APPROACH TO PERFLUOROCHEMICALS: LIQUID PHASE PHOTOFLUORINATION WITH ELEMENTAL FLUORINE. PART I

Scherer, Kirby V.,Yamanouchi, Kouichi,Ono, Taizo

, p. 47 - 65 (1990)

This paper describes a novel, safe, effective technique, with a new reactor design, for the synthesis of perfluorochemicals.This method, the liquid-phase photofluorination with undiluted fluorine, is appicable to the preparative-scale synthesis of isomerically-pure branched F- alkanes, F-ethers and F-tert-amines which are difficult to prepare by the classical fluorination methods (i.e. electrochemical or CoF3).The technique is based on the controlled inverse addition of the materials to be fluorinated to a well-stirred F2-saturated inert solvent, with simultaneous UV irradiation.The application of this method to the synthesis of F-ethers is described: the following were made by this method, F-2-propoxy-2-methyl-pentane, F-2-isobutoxy-2-methylpentane, F-n-heptylpropylether, F-2-pentoxy-2-methoxypropane, F-3-propoxy-2-methylpentane, F-2-ethyl-2-isopropyltetrahydrofuran, F-3-isobutoxy-2-methylpentane, F-2-methoxy-4-ethyl-4-methylhexane, and F-2-methyl-(1-ethyl-1-methylpropyl)oxetane.

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