6627-93-6 Usage
Uses
Used in Dyes and Pigments Industry:
3-AMINO-5-HYDROXY-4-PHENYLAZOPYRAZOLE is used as a colorant in the dyes and pigments industry for its ability to impart specific hues and shades to various materials. Its chemical structure allows for a wide range of color options, making it a versatile compound for use in this industry.
Used in Pharmaceutical Research:
3-AMINO-5-HYDROXY-4-PHENYLAZOPYRAZOLE is used as a research compound in the pharmaceutical industry due to its potential biological activities. Its structure suggests that it may possess antioxidant and anti-inflammatory properties, which could be harnessed for the development of new drugs and therapies.
Used in Antioxidant Applications:
3-AMINO-5-HYDROXY-4-PHENYLAZOPYRAZOLE is used as an antioxidant agent for its potential to neutralize free radicals and protect cells from oxidative damage. This property makes it a promising candidate for use in various health and wellness products, as well as in the development of new pharmaceuticals.
Used in Anti-Inflammatory Applications:
3-AMINO-5-HYDROXY-4-PHENYLAZOPYRAZOLE is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms associated with various inflammatory conditions. Further research is needed to fully understand and exploit its anti-inflammatory properties for use in medical treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 6627-93-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6627-93:
(6*6)+(5*6)+(4*2)+(3*7)+(2*9)+(1*3)=116
116 % 10 = 6
So 6627-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N5O/c10-8-7(9(15)14-13-8)12-11-6-4-2-1-3-5-6/h1-5,11H,(H3,10,12,13,14,15)
6627-93-6Relevant academic research and scientific papers
Reaction of (chloro carbonyl) phenyl ketene with 5-amino pyrazolones: Synthesis, characterization and theoretical studies of 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives
Zahedifar, Mahboobeh,Razavi, Razieh,Sheibani, Hassan
, p. 730 - 735 (2016/07/26)
New 7-hydroxy-6-phenyl-3-(phenyldiazenyl)pyrazolo[1,5-a]pyrimidine-2,5(1H,4H)-dione derivatives were synthesized from the reaction of (chlorocarbonyl)phenyl ketene and 5-amino pyrazolones in high to excellent yields and short reaction times. Structures of
Chemoselective three component reactions of 3-aminopyrazoles, aldehydes and malononitrile: Optimize the structures and compute the energies of possible tautomers
Sheibani, Hassan,Saheb, Vahid,Rezaei, Marjan,Zahedifar, Mahboobeh
, p. 126 - 130 (2014/03/21)
A chemoselective synthesis of 7-amino-5-aryl-2-hydroxy-3- (aryldiazenylpyrazolo[1,5-α]pyrimidine-6- carbonitriles and 4-((7-amino-6-cyano-2-hydroxy-5-arylpyrazolo[1,5-α]pyrimidine-3-yl) diazenyl)benzenesulfonamides through three-component reaction of 3-am
Synthesis of Azoles and Fused Azoles from α-Arylhydrazononitriles
Ibrahim, Mohamed Kamal Ahmed,El-Moghayar, Mohamed Riffat Hamza
, p. 832 - 835 (2007/10/02)
The reaction of α-arylhydrazononitriles (I) with phenylhydrazine, hydrazine hydrate, p-phenylenediamine, mercaptoacetic acid, and phenyl isothiocyanate gives amidrazone (IIa-c, III), pyrazolone (IVa-c), benzimidazole (X), 4-thiazolone (XIe,d) and 1,2,4-tr