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Phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate is a complex chemical compound that is primarily recognized for its role as a dye in various industries. It is characterized by a phenyl group linked to a benzenesulphonate molecule, with a cyano group and a dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridylazo group bridging the two. The unique color properties of phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate are attributed to the presence of the azo group, which is a key structural feature in many dyes.

72152-88-6

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72152-88-6 Usage

Uses

Used in Textile Industry:
Phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate is used as a dyeing agent for imparting vibrant colors to fabrics. Its application in this industry is due to its ability to produce a wide range of hues, enhancing the visual appeal of textiles.
Used in Printing Industry:
In the printing industry, phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate is used as a colorant to ensure the production of high-quality prints with consistent and long-lasting color. Its stability and colorfastness make it a preferred choice for various printing applications.
Used in Chemical Research:
Phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate may also be utilized in chemical research as a compound of interest due to its intricate molecular structure. Researchers may explore its potential interactions with other compounds and its behavior under different conditions.
Used in Biological Research:
In biological research, phenyl 4-[[5-cyano-1,6-dihydro-2-hydroxy-1-(3-methoxypropyl)-4-methyl-6-oxo-3-pyridyl]azo]benzenesulphonate could be employed as a tool to study biological systems, particularly where its unique chemical properties can be leveraged to investigate cellular processes or interactions with biomolecules.

Check Digit Verification of cas no

The CAS Registry Mumber 72152-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,1,5 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72152-88:
(7*7)+(6*2)+(5*1)+(4*5)+(3*2)+(2*8)+(1*8)=116
116 % 10 = 6
So 72152-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H22N4O6S/c1-16-20(15-24)22(28)27(13-6-14-32-2)23(29)21(16)26-25-17-9-11-19(12-10-17)34(30,31)33-18-7-4-3-5-8-18/h3-5,7-12,25H,6,13-14H2,1-2H3/b26-21-

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