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6613-46-3

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6613-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6613-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6613-46:
(6*6)+(5*6)+(4*1)+(3*3)+(2*4)+(1*6)=93
93 % 10 = 3
So 6613-46-3 is a valid CAS Registry Number.

6613-46-3SDS

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 methyl 2-(1-benzyl-2-oxoindol-3-ylidene)-5-(4-methoxyphenyl)-7-methyl-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

1.2 Other means of identification

Product number -
Other names methyl (2Z)-2-(1-benzyl-2-oxoindol-3-ylidene)-5-(4-methoxyphenyl)-7-methyl-3-oxo-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate

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:6613-46-3 SDS

6613-46-3Relevant articles and documents

Solvent effects on the energetics of intermolecular charge-transfer reactions

O'Driscoll, Erin,Simon, John D.,Peters, Kevin S.

, p. 7091 - 7098 (2007/10/02)

Picosecond absorption spectroscopy is used to examine the intermolecular electron-transfer reaction between the trans-stilbene radical cation and a series of olefin radical anions in polar solvents. Laser excitation of a ground-state complex between trans-stilbene and electron-deficient olefins selectively generates the contact ion pair within the time resolution of the experiment. By monitoring the time-dependent absorption of the trans-stilbene radical cation, the dynamics of electron back-transfer and ion-pair separation are studied. The rate of electron back-transfer is found to be temperature independent in the series of polar aprotic solvents over the temperature range from -8 °C to +80 °C. However, a linear correlation is observed between the charge-transfer rate and solvent polarity. With this result, the temperature data are interpreted in terms of solvent polarity effects on the activation energy for charge transfer. Once the rates are corrected for variation of solvent polarity, activation parameters are determined and the contributions of solvation and intramolecular modes to the reorganizational energy are evaluated. The dynamics of ion-pair separation are also briefly discussed.

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