39645-73-3 Usage
Description
(dibutylcarbamimidoyl)selanyl, also known as DBCIMS, is an organoselenium compound characterized by the presence of a carbamimidoyl (or amidine) group and a dibutyl substituent. With the chemical formula C10H22N2Se, it is recognized for its potential applications in therapeutics, particularly in cancer treatment, and as an antioxidant with protective effects against oxidative stress and inflammation. Its versatility extends to the synthesis of organic compounds and as a catalyst in chemical reactions, making it a compound of significant interest for research and exploration.
Uses
Used in Pharmaceutical Applications:
(dibutylcarbamimidoyl)selanyl is used as a therapeutic agent for its potential in treating cancer and other diseases. Its application is based on its ability to exhibit protective effects against oxidative stress and inflammation, which are often associated with the pathogenesis of various diseases.
Used in Antioxidant Applications:
In the field of antioxidant research, (dibutylcarbamimidoyl)selanyl is used to counteract oxidative stress, a process that can lead to cellular damage and contribute to the development of various diseases. Its antioxidant properties make it a promising candidate for further study and potential use in the prevention or treatment of conditions related to oxidative stress.
Used in Chemical Synthesis:
(dibutylcarbamimidoyl)selanyl is utilized in the synthesis of organic compounds, taking advantage of its unique chemical structure and reactivity. This application is based on its potential to facilitate the creation of new molecules with specific properties and functions.
Used as a Catalyst in Chemical Reactions:
(dibutylcarbamimidoyl)selanyl is also used as a catalyst to enhance the efficiency of certain chemical reactions. Its role as a catalyst is attributed to its ability to lower the activation energy required for a reaction to proceed, thus increasing the reaction rate and improving the overall process.
Overall, (dibutylcarbamimidoyl)selanyl is a multifaceted compound with a range of potential applications across different industries, including pharmaceuticals, antioxidants, chemical synthesis, and catalysis, making it a valuable subject for ongoing research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 39645-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39645-73:
(7*3)+(6*9)+(5*6)+(4*4)+(3*5)+(2*7)+(1*3)=153
153 % 10 = 3
So 39645-73-3 is a valid CAS Registry Number.
39645-73-3Relevant articles and documents
PHOTOSENSITIZING MEROCYANINE DYES BASED ON SELENOBARBITURIC ACID
Guenther, Wolfgang H. H.,Searle, Roger,Sieber, Fritz
, p. 417 - 424 (2007/10/02)
Structural analogs of Merocyanine 540 (MC540) were synthesized to probe biological mechanisms of action and to enhance viral inactivation.Novel pyrimidine-2-selone analogs of known and modified merocyanine sensitizers are described.A surprising result of placing selenium at the barbiturate site was the ca. 100-fold enhancement of photogeneration efficiency for singlet oxygen (1O2).Conversely, selenium directly attached to the chromophore ?-system was much less efficacious.The production of more 1O2 is reflected in greatly improved biological effectiveness of the new dyes.A puzzling high to low bioactivity isomer effect among molecules containing naphthoxazole or naphthothiazole components is shown by both thione and selone dyes.
