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1-Penten-3-one, 4,4,5,5-tetrafluoro-1-mercapto-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64249-79-2

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64249-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64249-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,4 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64249-79:
(7*6)+(6*4)+(5*2)+(4*4)+(3*9)+(2*7)+(1*9)=142
142 % 10 = 2
So 64249-79-2 is a valid CAS Registry Number.

64249-79-2SDS

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-tetrafluoro-1-phenyl-1-sulfanylpent-1-en-3-one

1.2 Other means of identification

Product number -
Other names 1-Phenyl-4,4,5,5-tetrafluor-1-mercapto-pent-1-en-3-on

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:64249-79-2 SDS

64249-79-2Downstream Products

64249-79-2Relevant academic research and scientific papers

THERMODYNAMIC AND KINETIC CHRACTERISTICS OF THE ENOL-ENETHIOL EQUILIBRIUM IN POLYFLUORINATED MONOTHIO 1,3-DIKETONES ACCORDING TO PMR SPECTROSCOPY

Gindin, V. A.,Nikol'skii, A. L.,Ershov, B. A.,Kol'tsov, A. I.,Pashkevich, K. I.

, p. 1765 - 1769 (2007/10/02)

The effect of structural factors on the position of the enol-enethiol equilibrium, the thermodynamic parameters, and the interconversion rate of the tautomers was investgated in the series of polyfluorinated monothio 1,3-ketones (RFCOCH2CSR, where RF = CF3, H(CF2)2; R = Alk, Ph) by PMR spectroscopy.At temperatures below -70 deg C the individual PMR spectra of these forms were recorded in a number of cases.It was established that increase in the size of the substituent R shifts the equilibrium substantially toward the enolic form but has little effect on the interconversion rate of the tautomers.

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