86-45-3 Usage
Uses
Used in Biochemical and Molecular Biological Research:
5-amino-6-methoxynaphthalene-2-sulphonic acid serves as a fluorescent labeling agent for the detection and visualization of proteins and nucleic acids. Its fluorescent properties allow for the tracking and analysis of these biomolecules in various experimental setups.
Used as a Precursor in Dye and Pharmaceutical Synthesis:
Due to its chemical structure, 5-amino-6-methoxynaphthalene-2-sulphonic acid is utilized as a starting material in the synthesis of dyes and pharmaceuticals. Its unique functional groups contribute to the development of new compounds with specific properties and applications.
Used in Sensor and Analytical Application Development:
5-amino-6-methoxynaphthalene-2-sulphonic acid's fluorescent properties and biomolecule interaction capabilities make it a promising candidate for the development of sensors and other analytical tools. These applications can leverage its ability to bind with specific targets or change its fluorescence upon interaction, enabling sensitive and selective detection methods.
Check Digit Verification of cas no
The CAS Registry Mumber 86-45-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86-45:
(4*8)+(3*6)+(2*4)+(1*5)=63
63 % 10 = 3
So 86-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4S/c1-16-10-5-2-7-6-8(17(13,14)15)3-4-9(7)11(10)12/h2-6H,12H2,1H3,(H,13,14,15)
86-45-3Relevant academic research and scientific papers
Bisazo brown reactive dye
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, (2008/06/13)
A brown reactive dye represented by a free acid of the formula, STR1 wherein R is a hydrogen atom or a C1 to C4 alkyl group, X is --SO2 CH2 CH2 Cl, --SO2 CH=CH2, --SO2 CH2 CH2 OSO3 H or --SO2 CH2 CH2 OPO3 H2, rings A, B and C are each a benzene or naphthalene ring which may have other substituent, m is 0 to 3 and n is 0 to 1. This dye is suitable for dyeing cellulose fibers brown to afford dyeings superior in fastnesses, acid stability, build-up property and level dyeing property.
Reactive yellow dye having both monochlorotriazinyl and vinylsulfone type reactive groups
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, (2008/06/13)
The compounds represented, in the form of free acid, by the following general formula (I): STR1 (wherein A is STR2 (wherein R3 and R4 are each hydrogen or a methyl, ethyl, methoxy, ethoxy, acetylamino, propionylamino, benzoylamino or ureido group, and R5 and R6 are each hydrogen or a methyl or methoxy group), R1 and R2 are each hydrogen or a methyl, ethyl or sulfomethyl group, X1 and X2 are each hydrogen, chlorine or a methyl, methoxy, carboxyl or sulfonic acid group, m is a number of 0, 1 or 2, and n is a number of 1 or 2, provided that the sum of m and n is 1, 2 or 3). These compounds are capable of dyeing cellulose fibers in yellow with excellent color fastness to hypochlorite, light, perspiration and sunlight and high acid stability.
