301681-73-2 Usage
Heterocyclic compound
Yes
It contains a benzoxathiol ring, which is a heterocyclic ring consisting of carbon, sulfur, and oxygen atoms.
Benzoxathiol ring
Present
The compound has a benzoxathiol ring, which is a six-membered aromatic ring with one sulfur and one oxygen atom.
Hydroxy group
Present at the 5-position
The compound contains a hydroxy group (-OH) attached to the 5th position of the benzoxathiol ring.
Chlorophenyl substituent
Present at the 7-position
A chlorophenyl group (a phenyl ring with a chlorine atom) is attached to the 7th position of the benzoxathiol ring.
Pharmacological and therapeutic properties
Potential
The compound may have potential applications in the development of pharmaceutical drugs due to its unique structure and properties.
Research interest
High
Its structure and properties make it of interest for research and potential application in the fields of medicine and drug development.
Application
Potential use in medicine and drug development
Due to its pharmacological and therapeutic properties, the compound may be used in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 301681-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,6,8 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 301681-73:
(8*3)+(7*0)+(6*1)+(5*6)+(4*8)+(3*1)+(2*7)+(1*3)=112
112 % 10 = 2
So 301681-73-2 is a valid CAS Registry Number.
301681-73-2Relevant academic research and scientific papers
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.
