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64806-62-8

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64806-62-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64806-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64806-62:
(7*6)+(6*4)+(5*8)+(4*0)+(3*6)+(2*6)+(1*2)=138
138 % 10 = 8
So 64806-62-8 is a valid CAS Registry Number.

64806-62-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylpropyl 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names Dihydrocinnamyltrifluoracetat

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:64806-62-8 SDS

64806-62-8Relevant articles and documents

Synthesis of terminal perfluoroalkyl enol ethers and epoxy ethers

Begue, Jean-Pierre,Bonnet-Delpon, Daniele,Kornilov, Andrei

, p. 1057 - 1063 (1996)

A practical method for the multigram-scale preparation in good yields of terminal perfluoroalkyl enol ethers, using Wittig olefination of perfluoroalkyl ethers, is reported. The corresponding epoxy ethers are available via their m-CPBA epoxidation in good

A Simple Preparation of Alkyl Trifluoromethanesulfonates (Triflates) from Alkyl Trimethylsilyl Ethers

Aubert, Corinne,Begue, Jean-Pierre

, p. 759 - 760 (2007/10/02)

Several alkyl trifluoromethanesulfonates (triflates) 2 are prepared by reacting alkyl trimethylsilyl ethers 1 with trifluoromethanesulfonic anhydride.The triflates 2 can be used for further reactions without isolation, as illustrated in the preparation of the ether 3 and cumene (4).

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