4671-93-6 Usage
Description
BENZYL SELENOCYANATE is a synthetic chemopreventative agent that possesses the ability to inhibit protein kinase A and protein kinase C. It is a compound with potential applications in various industries due to its unique properties and functions.
Uses
Used in Pharmaceutical Industry:
BENZYL SELENOCYANATE is used as a chemopreventative agent for its ability to inhibit protein kinase A and protein kinase C. This makes it a promising candidate for the development of treatments and therapies aimed at preventing the onset or progression of various diseases, particularly those related to abnormal cell growth and cancer.
Used in Research and Development:
In the field of research and development, BENZYL SELENOCYANATE is utilized as a valuable tool for studying the roles and mechanisms of protein kinase A and protein kinase C in cellular processes. This can lead to a better understanding of these enzymes and their involvement in various diseases, potentially paving the way for the development of new therapeutic strategies and targeted treatments.
Used in Drug Discovery:
BENZYL SELENOCYANATE's inhibitory effects on protein kinase A and protein kinase C make it a potential starting point for the development of new drugs targeting these enzymes. Researchers can use this compound as a lead molecule to design and synthesize more potent and selective inhibitors, which could be used in the treatment of various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 4671-93-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4671-93:
(6*4)+(5*6)+(4*7)+(3*1)+(2*9)+(1*3)=106
106 % 10 = 6
So 4671-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NSe/c9-7-10-6-8-4-2-1-3-5-8/h1-5H,6H2
4671-93-6Relevant articles and documents
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Pan,W.-H.,Fackler,J.P.
, p. 5783 - 5789 (1978)
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(1-Selenocyanatoethyl)benzene: A Selenocyanation Reagent for Site-Selective Selenocyanation of Inert Alkyl C(sp3)-H Bonds
Yu, Fei,Li, Chuang,Wang, Chuangye,Zhang, Hongwei,Cao, Zhong-Yan
supporting information, p. 7156 - 7160 (2021/09/18)
A new, simple, yet easily accessible, (1-selenocyanatoethyl)benzene has been designed and applied as a SeCN group transfer reagent for selenocyanation of aliphatic C(sp3)-H bonds for the first time. This protocol is featured with mild reaction conditions and wide substrate scope. Control experiments reveal that a radical-group transfer mechanism might be involved.
AIBN-initiated direct thiocyanation of benzylic sp3C-H with: N -thiocyanatosaccharin
Wu, Di,Duan, Yongjie,Liang, Kun,Yin, Hongquan,Chen, Fu-Xue
supporting information, p. 9938 - 9941 (2021/10/12)
Direct thiocyanations of benzylic compounds have been implemented. Here, a new strategy, involving a free radical reaction pathway initiated by AIBN, was used to construct the benzylic sp3 C-SCN bond. In this way, the disadvantage of other strategies involving introducing leaving groups in advance to synthesize benzyl thiocyanate compounds was overcome. The currently developed protocol also involved the use of readily available raw materials and resulted in high product yields (up to 100%), both being great advantages for synthesizing benzyl thiocyanates.