77203-71-5 Usage
Uses
Used in Laboratory Applications:
2,4-dibromo-6-[(6-methyl-1,3-benzothiazol-2-yl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a pH indicator in laboratory settings for its ability to change color in response to different pH levels, aiding in the accurate measurement and assessment of acidity or alkalinity in solutions.
Used in Textile Industry:
In the textile industry, 2,4-dibromo-6-[(6-methyl-1,3-benzothiazol-2-yl)amino]methylidenecyclohexa-2,4-dien-1-one is used as a dye for silk and wool, capitalizing on its vibrant color to enhance the appearance of these natural fibers.
Used in Biological Staining:
2,4-dibromo-6-[(6-methyl-1,3-benzothiazol-2-yl)amino]methylidenecyclohexa-2,4-dien-1-one is also utilized as a biological stain in laboratory research, where its color-changing properties can help in the visualization and differentiation of cellular structures and organisms under microscopic examination.
Check Digit Verification of cas no
The CAS Registry Mumber 77203-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,0 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77203-71:
(7*7)+(6*7)+(5*2)+(4*0)+(3*3)+(2*7)+(1*1)=125
125 % 10 = 5
So 77203-71-5 is a valid CAS Registry Number.
77203-71-5Relevant academic research and scientific papers
Synthesis and Biological Activity of Some Schiff Bases Derived from Thiazoles and Benzothiazoles
Dash, B.,Patra, M.,Praharaj, S.
, p. 894 - 897 (2007/10/02)
4-Aryl-2-aminothiazoles and 2-aminobenzothiazoles undergo condensation with salicylaldehyde in the presence of piperidine to give the schiff bases II and III, respectively.A similar reaction of 4-aryl-2-aminothiazole methiodides gives the schiff bases 4-aryl-2-(2'-hydroxyaryliminomethyl)thiazole methiodides (IV).Several schiff bases have been condensed with cyclohexanone and thioglycollic acid to furnish 4-aryl-2-(2'-hydroxy-α-substituted benzylamino)thiazoles (V) and 2-(2'-hydroxyphenyl) or naphthyl)-3-(4''-arylthiazol-2''-yl)-4-thiazolidones (VI), respectively.Structure elucidation of the schiff bases has been made on the basis of their elemental analyses, IR and mass spectral data.The biological screening data of the schiff bases and their metal complexes are also presented.
