55212-06-1 Usage
Bicyclic ring structure
2,3-dihydro-5H-4,1-benzoxathiepin-5-one has a ring structure consisting of two cyclic rings.
Contains oxygen and sulfur atoms
2,3-dihydro-5H-4,1-benzoxathiepin-5-one contains two different heteroatoms, oxygen and sulfur, which contribute to its unique chemical properties.
Heterocyclic compound
2,3-dihydro-5H-4,1-benzoxathiepin-5-one is a heterocyclic compound, meaning it contains at least one ring structure with atoms other than carbon.
Member of the benzoxathiepine family
2,3-dihydro-5H-4,1-benzoxathiepin-5-one belongs to a specific group of compounds called benzoxathiepine, which share a similar structure and properties.
Potential applications in pharmacology and medicinal chemistry
2,3-dihydro-5H-4,1-benzoxathiepin-5-one has potential therapeutic properties and can be used in the development of new drugs for the treatment of various medical conditions.
Building block for the synthesis of various pharmaceuticals and chemical compounds
2,3-dihydro-5H-4,1-benzoxathiepin-5-one can be used as a starting material for the synthesis of other compounds, making it a valuable building block in the field of chemistry.
Potential use in the development of new drugs
2,3-dihydro-5H-4,1-benzoxathiepin-5-one has the potential to be used in the development of new drugs for the treatment of various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 55212-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55212-06:
(7*5)+(6*5)+(5*2)+(4*1)+(3*2)+(2*0)+(1*6)=91
91 % 10 = 1
So 55212-06-1 is a valid CAS Registry Number.
55212-06-1Relevant academic research and scientific papers
Cu-Mediated C-H Thioetherification of Arenes at Room Temperature
Wang, Xing,Yi, Xing,Xu, Hui,Dai, Hui-Xiong
supporting information, p. 5981 - 5985 (2019/08/26)
Cu-mediated C-H thioetherification of arenes with ethylene sulfide has been developed using a readily removable directing group. The reaction proceeded at room temperature, and a variety of sensitive functional groups including chloro, bromo, and vinyl were well tolerated. The thiolated products could be converted to the seven-membered benzoxathiepinones derivatives by a sequence of hydrolysis-lactonization reactions.
