25625-01-8 Usage
Uses
Used in Organic Synthesis:
Benzo[b]thiophen-3(2H)-one, 2-(phenylmethylene)-, 1,1-dioxide is used as a key intermediate in the synthesis of various organic compounds due to its ability to participate in nucleophilic substitutions, electrophilic additions, and oxidative transformations.
Used in Medicinal Chemistry:
Benzo[b]thiophen-3(2H)-one, 2-(phenylmethylene)-, 1,1-dioxide is used as a building block for the development of new drugs and biologically active molecules, leveraging its anticancer, antimicrobial, and antioxidant properties.
Used in Drug Development:
Benzo[b]thiophen-3(2H)-one, 2-(phenylmethylene)-, 1,1-dioxide is used as a potential therapeutic agent for the treatment of various diseases, given its demonstrated biological activities and the opportunities it presents for the design of novel chemical entities with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25625-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,6,2 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25625-01:
(7*2)+(6*5)+(5*6)+(4*2)+(3*5)+(2*0)+(1*1)=98
98 % 10 = 8
So 25625-01-8 is a valid CAS Registry Number.
25625-01-8Relevant academic research and scientific papers
Elimination, ring-contraction, and fragmentation reactions of 1-thioflavanone 1-oxides
Somogyi
, p. 1159 - 1165 (2007/10/03)
Epimeric thioflavanone sulfoxides (2b) were selectively transformed into thioflavone (1a), thioaurone (3a), and di(2-cinnamoylphenyl) disulfide (4). Disulfide 4 can be recyclized into thioaurones (3a-c) and thioflavanones (2a, 5) with heterolysis of the S - S bond. The 3-p-anisylidene sulfoxide analog of 2b (6) transforms, with fragmentation, into 4′-methoxythioaurone 3b.
Dioxirane Oxidation of (Z)-1-Thioaurones, (E)-3-Arylidene-1-thiochroman-4-ones and (E)-3-Arylidene-1-thioflavan-4-ones
Adam, Waldemar,Golsch, Dieter,Hadjiarapoglou, Lazaros,Levai, Albert,Nemes, Csaba,Patonay, Tamas
, p. 13113 - 13120 (2007/10/02)
The oxidation of the title compounds 1, 4 and 7 with dimethyldioxirane (DMD) afforded the corresponding sulfoxides 2, 5 and 8 and/or sulfones 3, 6 and 9 in good yields (Scheme 1 and 2).Excess dimethyldioxirane gave the sulfones chemoselectively without fo
