38901-87-0 Usage
Uses
Used in Chemical Synthesis:
2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] is used as a reagent or intermediate in organic synthesis for its unique reactivity and properties. It aids in the formation of various complex organic molecules, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] is being researched for its potential medicinal properties. Its unique chemical structure may offer new avenues for the development of pharmaceuticals, particularly in the areas of drug discovery and design.
Used in Analytical Chemistry:
2,5-Cyclohexadiene-1,4-dione,
mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] can also be utilized in analytical chemistry as a tool for detecting or analyzing other substances due to its specific reactivity. It may be employed in the development of new analytical methods or the improvement of existing ones, enhancing the sensitivity and selectivity of chemical analyses.
Used in Material Science:
2,5-Cyclohexadiene-1,4-dione, mono[(3-methyl-2(3H)-benzothiazolylidene)hydrazone] may have applications in material science, where its unique properties could be leveraged to develop new materials with specific characteristics. This could include the creation of novel polymers, coatings, or other materials with tailored properties for various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 38901-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,0 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38901-87:
(7*3)+(6*8)+(5*9)+(4*0)+(3*1)+(2*8)+(1*7)=140
140 % 10 = 0
So 38901-87-0 is a valid CAS Registry Number.
38901-87-0Relevant academic research and scientific papers
Nucleophilic Aromatic Substitution: Effect of Complexation on the Alkaline Hydrolysis of 4-Aminophenylazobenzothiazolium Dyes
D'Rozario, Augustine P.,Williams, Andrew,Parton, Brian
, p. 1785 - 1788 (2007/10/02)
Nucleophilic attack by hydroxide ion on 2-(4-dimethylaminophenylazo)-3,6-dimethylbenzothiazolium iodide to expel the dimethylamino function is inhibited in aqueous solution by aromatic carboxylate, aromatic sulphonate, and phenolate ions.The inhibition is demonstrated to involve complexation of dye with solute to form an unreactive species.The dissociation constant of the complex is relatively insensitive to structure except in the case of phenolate ions where electron withdrawing substituents favour stability.Both charge transfer and electrostatic effects are necessary for efficient complexing ability of the additive.Complexation of cyclodextrin with the dye is followed by reaction to yield a dye-cyclodextrin covalent species; the intermediate slowly decomposes to give quinone imine, the regular product of dye hydrolysis.
NUCLEOPHILIC AROMATIC SUBSTITUTION: FADING OF BENZOTHIAZOLIUM AZO DYES IN ALKALINE SOLUTION
D'Rozario, Augustine P.,Parton, Brian,Williams, Andrew
, p. 395 - 400 (2007/10/02)
Benzothiazolium azo dyes bearing a 4'-amino function hydrolyse in alkali according to the equation:.The reaction is catalysed by amines; a dye with R1=CH2CH2OH exhibits a third-order kinetic term (k3->) which is not observed with dyes without a hydroxyl group in R1 or R2.Methoxide ion gives reversible formation of a ?-bonded adduct with the dyes; benzothiazolium azo dyes with weakly basic amine substituents react with hydroxide ion to form adducts which regenerate the azo dye on addition of acid.
