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64576-54-1

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64576-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64576-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,7 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64576-54:
(7*6)+(6*4)+(5*5)+(4*7)+(3*6)+(2*5)+(1*4)=151
151 % 10 = 1
So 64576-54-1 is a valid CAS Registry Number.

64576-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5Z)-3,4-dimethyl-5-(pyridin-2-ylmethylidene)pyrrol-2-one

1.2 Other means of identification

Product number -
Other names Z-3,4-dimethyl-5-(2-pyridylmethylidene)-3-pyrrolin-2-one

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:64576-54-1 SDS

64576-54-1Downstream Products

64576-54-1Relevant articles and documents

SYNTHESIS AND PROPERTIES OF 2,2'-PYRROMETHENE-5(1H)-ONE ANALOGUES: THE FURAN, THIOPHENE, BENZENE, 4-METHOXYBENZENE, 2-PYRIDINE AND 4-PYRIDINE ANALOGUES

Groot, J. A. de,Jansen, H.,Fokkens, R.,Lugtenburg, J.

, p. 114 - 118 (2007/10/02)

Condensation of furfural, thiophene-2-carboxaldehyde, benzaldehyde, 4-methoxy-benzaldehyde, pyridine-2-carboxaldehyde and pyridine-4-carboxaldehyde with 3,4-dimethyl-3-pyrrolin-2-one leads to the Z-2,2'-pyrromethene-5(1H)-one analogues.Following irradiation with light, the E forms have been isolated and characterized.Complete thermal E -> Z isomerisation is observed upon heating in basic methanol.On irradiation in non hydrogen-donating solvents the analogues 3a, 3b and 3e show very little or no photoisomerisation due to the intramolecular hydrogen bond.Condensation of these aldehydes with 1,3,4-trimethyl-3-pyrrolin-2-one gives mixtures of the corresponding Z- and E-2,2'-pyrromethene-5(1H)-one analogues.The Z and E forms both isomerise thermally upon heating in basic methanol to give the same equilibrium state as is observed during the synthesis.Upon irradiation with light, the compounds similarly undergo Z-E isomerisation.

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