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79009-23-7

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79009-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79009-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,0 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79009-23:
(7*7)+(6*9)+(5*0)+(4*0)+(3*9)+(2*2)+(1*3)=137
137 % 10 = 7
So 79009-23-7 is a valid CAS Registry Number.

79009-23-7SDS

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 3-(2-benzothiazolyl)-7-(N-phenylsulfonyl)aminocoumarin

1.2 Other means of identification

Product number -
Other names N-(3-Benzothiazol-2-yl-2-oxo-2H-chromen-7-yl)-benzenesulfonamide

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:79009-23-7 SDS

79009-23-7Relevant articles and documents

Synthesis and Spectral Properties of 7-(N-Arylsulfonyl)aminocoumarins, A New Class of Fluorescent pH Indicators

Wolfbeis, Otto S.,Baustert, John H.

, p. 1215 - 1218 (2007/10/02)

7-Arylsulfonylamino-coumarins 3 and 5, with electron-delocalizing substituents in position 3 were obtained by condensation of 4-arylsulfonylamino-2-hydroxybenzaldehyde with various (hetero)arylacetic esters and by other methods.Oxidative cyanation using potassium cyanide and elemental bromine gave the corresponding 4-cyano derivatives 6a,b. The absorption and emission maxima of coumarins 3 and 5 in organic solvents and in water of different pH were determined.All showed bright blue fluorescence in organic or acidic aqueous solution, which is shifted to the green in alkaline solution.The 4-cyano derivatives 6a,b exhibit green fluorescences, which change to yellow in alkaline solution.Simultaneously the color changes from yellow to orange. The pKa values of compounds 3 and 5 were found to lie between 6.33 and 7.06, whereas for the 4-cyano derivatives they were distinctly lower (5.66-5.95).The spectral changes observed in the near neutral pH range may render the new compounds useful indicators for the measurement of physiological pH's.

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