5084-13-9 Usage
Molecular structure
1-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)-2'-tetradecyloxy-2-naphthanilide consists of a naphthalene core with a hydroxyl group, a tetrazole ring, and a tetradecyloxy chain attached to it.
Class of compound
It belongs to the class of naphthol AS dyes, which are known for their coloring properties.
Industrial applications
1-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)-2'-tetradecyloxy-2-naphthanilide is used as a coloring agent in various industries such as textiles, inks, and plastics.
Functional groups
The presence of a hydroxyl group (-OH), a tetrazole ring (1H-tetrazol-5-yl), and a tetradecyloxy chain (2'-tetradecyloxy) give 1-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)-2'-tetradecyloxy-2-naphthanilide its unique properties and functionality.
Synthetic origin
It is a synthetic substance, meaning it is man-made and not naturally occurring.
Potential applications
Due to its complex structure, 1-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)-2'-tetradecyloxy-2-naphthanilide may have potential uses in pharmaceuticals, polymers, and other research and development areas.
Further research needed
The specific uses and effects of 1-hydroxy-4-(1-phenyl-1H-tetrazol-5-ylthio)-2'-tetradecyloxy-2-naphthanilide would require additional studies and investigations to be fully understood and determined.
Check Digit Verification of cas no
The CAS Registry Mumber 5084-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5084-13:
(6*5)+(5*0)+(4*8)+(3*4)+(2*1)+(1*3)=79
79 % 10 = 9
So 5084-13-9 is a valid CAS Registry Number.
5084-13-9Relevant academic research and scientific papers
Process for preparation of 4-mercapto-1-naphthol compounds
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, (2008/06/13)
A process for preparation of 4-mercapto-1-naphthol compounds which comprises the steps of: (i) obtaining a 4-heterocyclylthio-1-naphthol compound by reacting a 1-naphthol compound with a heterocyclylsulfur chloride or by reacting a 4-iodo-1-naphthol compound with an alkali metal or ammonium salt of a mercaptoheterocyclic compound, (ii) hydrolyzing the resulting 4-heterocyclylthio-1-naphthol compound in the presence of a base to form a reaction product, and (iii) acidifying said reaction product. The resulting compounds are useful as intermediates in the synthesis of bleach accelerator releasing couplers for use in silver halide color photographic materials.
