6085-98-9 Usage
Molecular structure
The compound has a complex structure containing thiazole, benzimidazole, and naphthalene moieties.
Type of compound
It is a sulfonate ester derivative.
Potential applications
The compound is potentially useful for various applications in organic synthesis, pharmaceuticals, and material science.
Sulfonate group
The presence of a sulfonate group can confer water solubility.
Biological activities
The presence of the thiazole and benzimidazole moieties suggests potential biological activities such as antimicrobial or anticancer properties.
Versatile starting material
The compound's specific chemical structure and properties make it a versatile starting material for the synthesis of various types of derivatives with potentially interesting properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6085-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6085-98:
(6*6)+(5*0)+(4*8)+(3*5)+(2*9)+(1*8)=109
109 % 10 = 9
So 6085-98-9 is a valid CAS Registry Number.
6085-98-9Relevant academic research and scientific papers
Azocoupling of Quaternary 1,2,4-Triazolium Salts to Form 5-p-N,N-Dimethylaminophenylazo-1,2,4-triazolium Salts
Becker, H. G. O.,Hoffmann, Gerda,Gwan, Kim Mun,Knuepfer, L.
, p. 325 - 337 (2007/10/02)
Quaternary 1,2,4-triazolium salts 1 couple easily with p-N,N-dimethylamino-benzenediazonium salts to form azodyes 3 (5-N,N-dimethylaminophenylazo-1,2,4-triazolium salts), preferably under solid-liquid phase transfer conditions using chloroform or methylene chloride and triethylamine or DABCO.Zwitterionic 1,2,4-triazolium salts (anhydro mercapto hydroxide, anhydro hydroxy hydroxide, and anhydro anilido hydroxide ("nitron")) couple as well.The azodyes - as also well known from industrially used types - absorb in the region of 500 nm and have high extinction coefficients.Substituents in 1-, 3- or 4-position of the triazolium ring exert no clear substituent effects.The quaternary 1,2,4-triazolium salts were synthesized according to standard procedures.
