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77820-11-2 Usage

Chemical Properties

yellow powder

Check Digit Verification of cas no

The CAS Registry Mumber 77820-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77820-11:
(7*7)+(6*7)+(5*8)+(4*2)+(3*0)+(2*1)+(1*1)=142
142 % 10 = 2
So 77820-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO3S/c1-3-19(4-2)13-8-7-12-10-14(18(21)22-15(12)11-13)17(20)16-6-5-9-23-16/h5-11H,3-4H2,1-2H3

77820-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Diethylamino-3-thenoylcoumarin

1.2 Other means of identification

Product number -
Other names 7-DIETHYLAMINO-3-THENOYLCOUMARIN

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:77820-11-2 SDS

77820-11-2Synthetic route

ethyl 2-thenoylacetate
13669-10-8

ethyl 2-thenoylacetate

4-(Diethylamino)salicylaldehyde
17754-90-4

4-(Diethylamino)salicylaldehyde

7-diethylamino-3-thenoylcoumarin
77820-11-2

7-diethylamino-3-thenoylcoumarin

Conditions
ConditionsYield
With piperidine In ethanol Heating;

77820-11-2Downstream Products

77820-11-2Relevant articles and documents

KETOCOUMARINS. A NEW CLASS OF TRIPLET SENSITIZERS

Specht, Donald P.,Martic, Peter A.,Farid, Samir,++

, p. 1203 - 1211 (2007/10/02)

Several derivatives of 3-ketocoumarins were prepared and are shown to have many of the photophysical criteria required for efficient triplet sensitizers.These compounds include 3-aroylcoumarins (1) and 3,3'-carbonyl-biscoumarins (2).The aryl groups in 1 are either phenyl and substituted phenyl derivatives or heterocyclic groups such as thienyl and benzofuryl.The substituents on the coumarin moiety in 1 and 2, if any, are alkoxy or dialkylamino.These compounds, with absorption maxima between 330 and 450 nm, have extinction coefficients in the range of 1E4 to almost 1E5, which is an important criterion for efficient sensitization of thin films of polymers as those used in photoresists and litography.The singlet-triplet intersystem crossing (isc) efficiencies of several derivatives approach unity.In others, however, a radiationless decay process competes with the isc.The decay process is particularly dominant in the assymetrically substituted derivatives of 2, but seems to be considerably supressed in polymeric matrices.The triplet energies of these compounds range from ca. 48 to 60 kcal/mol.Some of these ketocoumarins show phosphorescence spectra that suggest the presence of "frozen-in" rotamers.

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