37711-29-8 Usage
Description
ETHYL PHENOTHIAZINE-2-CARBAMATE is a chemical compound with the potential to influence the lifespan of eukaryotic organisms. It is utilized in various applications, particularly in the field of research and development, to study and understand the mechanisms that contribute to the aging process and to identify compounds that can potentially alter the lifespan of these organisms.
Uses
Used in Research and Development:
ETHYL PHENOTHIAZINE-2-CARBAMATE is used as a lifespan-altering compound for studying the aging process in eukaryotic organisms. Its application in this field is crucial for understanding the underlying mechanisms that contribute to aging and identifying potential targets for therapeutic interventions.
Used in Screening for Lifespan-Altering Compounds:
In the context of aging research, ETHYL PHENOTHIAZINE-2-CARBAMATE is employed as a tool for screening and identifying other compounds that may have the potential to alter the lifespan of eukaryotic organisms. This application is vital for the development of novel therapeutic strategies aimed at extending the healthy lifespan or improving the quality of life in various organisms, including humans.
Check Digit Verification of cas no
The CAS Registry Mumber 37711-29-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37711-29:
(7*3)+(6*7)+(5*7)+(4*1)+(3*1)+(2*2)+(1*9)=118
118 % 10 = 8
So 37711-29-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2O2S/c1-2-19-15(18)16-10-7-8-14-12(9-10)17-11-5-3-4-6-13(11)20-14/h3-9,17H,2H2,1H3,(H,16,18)
37711-29-8Relevant articles and documents
Preparation and pharmacological activities of 10-homolupinanoyl-2-R- phenothiazines
Sparatore,Sparatore
, p. 5 - 17 (2007/10/02)
Pursuing our researches on quinolizidinyl derivatives of phenothiazine and on the ground of antidepressive, diuretic, antianginal and antiarrhythmic activities of several 10-(3-dialkylamino) propionylphenothiazines (as chloracizine, moricizine, etc.), six
