1071-75-6 Usage
Description
S-PropylthiuroniuM BroMide is a chemical compound with potential applications in various fields, particularly due to its radio protective properties against x-rays.
Uses
Used in Pharmaceutical Industry:
S-PropylthiuroniuM BroMide is used as a radioprotective agent for its potential to protect cells and tissues from the harmful effects of x-rays. This application is particularly relevant in the context of radiation therapy for cancer patients, where it may help to minimize damage to healthy cells while maximizing the effectiveness of the treatment.
Used in Research and Development:
In addition to its potential pharmaceutical applications, S-PropylthiuroniuM BroMide may also be utilized in research and development settings to study the effects of radiation on biological systems. This could lead to a better understanding of the mechanisms underlying radiation-induced damage and the development of more effective radioprotective agents in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 1071-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1071-75:
(6*1)+(5*0)+(4*7)+(3*1)+(2*7)+(1*5)=56
56 % 10 = 6
So 1071-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2S.BrH/c1-2-3-7-4(5)6;/h2-3H2,1H3,(H3,5,6);1H
1071-75-6Relevant articles and documents
EFFECT OF VICINAL SUBSTITUENTS ON THE REACTIVITY IN BIMOLECULAR NUCLEOPHILIC SUBSTITUTION AT A SATURATED CARBON ATOM. TWO TYPES OF SUBSTITUENTS II. KINETICS OF THE REACTION OF THIOUREA WITH β-SUBSTITUTED BROMOETHANES IN ETHANOL
Ryazantsev, G. B.,Shaposhnikov, A. V.,Fedoseev, V. M.
, p. 1777 - 1782 (2007/10/02)
The kinetics of the reaction of thiourea with β-substituted bromoethanes in ethanol were studied by radiochromatography.The rate constants and activation parameters of the reactions were determined.It was shown that an isokinetic relationship is observed for the two types of substituents.The mechanisms of the effect of the vicinal substituents on the reactivity are discussed.
SYNTHESIS OF MONO(ALKYLTHIO)-SUBSTITUTED KETONES
Sabirov, S. S.,Gnevasheva, L. M.,Ismailov, M. I.,Isobaev, M. D.
, p. 1239 - 1243 (2007/10/02)
In the reaction of 2-propanone in the presence of sodium bicarbonate with a mixture of formaldehyde and the corresponding alkaline hydrolyzates of S-alkylthiuronium salts (thioalcoholates) β-keto sulfides (1-alkylthio-3-butanones) were obtained.Ketalization of the products with glycerol gave the cyclic derivatives alkylthio-1,3-dioxolanes.
