39645-73-3 Usage
General Description
(Dibutylcarbamimidoyl)selanyl, also known as DBCIMS, is an organoselenium compound containing a carbamimidoyl (or amidine) group and a dibutyl substituent. It has the chemical formula C10H22N2Se and is used in various chemical and biochemical applications. DBCIMS is known for its potential use as a therapeutic agent, particularly in the treatment of cancer and other diseases. It has also shown promise as an antioxidant and has been studied for its potential protective effects against oxidative stress and inflammation. Additionally, DBCIMS has been investigated for its potential use in the synthesis of organic compounds and as a catalyst in chemical reactions. Overall, (dibutylcarbamimidoyl)selanyl is a versatile compound with potential applications in various fields, making it an interesting subject of research and exploration.
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.
