327078-57-9 Usage
Chemical class
Belongs to the benzoxathiolone class
Heterocyclic compound
Contains a benzene ring fused to a thiolactone ring
Derivative
4-methylphenyl derivative, meaning it contains a phenyl group with a methyl substituent
Hydroxyl group
Presence of a hydroxyl group at the 5th position of the benzoxathiolone ring
Chemical properties
Unique chemical properties due to the hydroxyl group and the 4-methylphenyl substitution
Potential applications
Pharmaceutical and industrial applications
Further research
May be conducted to explore its potential uses and biological activities
Check Digit Verification of cas no
The CAS Registry Mumber 327078-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,0,7 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 327078-57:
(8*3)+(7*2)+(6*7)+(5*0)+(4*7)+(3*8)+(2*5)+(1*7)=149
149 % 10 = 9
So 327078-57-9 is a valid CAS Registry Number.
327078-57-9Relevant academic research and scientific papers
Synthesis of heterocycles on the basis of arylation products of unsaturated compounds: XX. Reaction of 2-aryl-1,4-benzoquinones with potassium O-butyl carbonodithioate
Martyak,Obushak,Matiichuk
experimental part, p. 394 - 398 (2010/09/12)
Reactions of 2-aryl-1,4-benzoquinones with potassium O-butyl carbonodithioate gave the corresponding 7-aryl-5-hydroxy-1,3-benzoxathiole-2- thiones. In some cases, 7-aryl-5-hydroxy-1,3-benzoxathiol-2-ones were also formed.
Synthesis of heterocycles based on products of anion arylation of unsaturated compounds. 5. Reaction of 2-aryl-1,4-benzoquinones with thiourea
Obushak,Matiichuk,Martyak
, p. 909 - 915 (2007/10/03)
2-Aryl-1,4-benzoquinones, that can be obtained by arylation of quinone by arenediazonium salts, regioselectively react with thiourea in acid medium to form 7-aryl-5-hydroxy-1,3-benzoxathiol-2-ones. In the presence of excess arylquinones at room temperature, 2-amino-6-hydroxybenzothiazoles are formed in the same reaction.
