39784-29-7 Usage
Description
1-(2-styrylphenyl)tetrazol-1-ium is a chemical compound that belongs to the tetrazolium family. It is a cation with an aromatic ring containing a styryl group and a tetrazolium group, known for its versatility in both research and medical fields.
Uses
Used in Biochemistry:
1-(2-styrylphenyl)tetrazol-1-ium is used as a redox indicator for assessing cell viability and proliferation. Its application reason is that it changes color in response to metabolic activity, making it useful for a variety of cell-based assays.
Used in Photodynamic Therapy:
In the medical field, 1-(2-styrylphenyl)tetrazol-1-ium is used as a potential photosensitizer. The application reason is that, when activated by light, it produces reactive oxygen species to destroy cancer cells.
Check Digit Verification of cas no
The CAS Registry Mumber 39784-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,8 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 39784-29:
(7*3)+(6*9)+(5*7)+(4*8)+(3*4)+(2*2)+(1*9)=167
167 % 10 = 7
So 39784-29-7 is a valid CAS Registry Number.
39784-29-7Relevant articles and documents
Vinyltetrazoles: III. Metal-catalyzed arylation, a new method of vinyltetrazoles functionalization
Aleshunin,Esikov,Dolgushin,Ostrovskii
, p. 1464 - 1472 (2013/05/21)
New functionalization procedure was developed for C- and N-vinyltetrazoles based on Heck reaction. Applying this method diverse (E)-styryl- and (E)-distyryltetrazoles were obtained for the first time in 76-85% yields. C-Vinyltetrazoles are more reactive in Heck cross-coupling than N-vinyltetrazoles. The arylation of 1-vinyltetrazole along Heck reaction proceeds with a C-H-activation and leads to the formation of 5-phenyl-1-[2-(E)-phenylethenyl]tetrazole.
