147895-43-0

Basic information

• Product Name: CarbaMiMidothioic acid, Methyl ester, sulfate
• Synonyms: 2-Methyl-2-thiopeudourea sulfate; 2-Methyl-2-thiopseudourea sulfate; S-Methylisothiuronium sulfate; S-Methylthiopseudourea sulfate; S-Methylthiouronium sulfate; Bis(S-methylthiouronium) sulphate; Pseudourea, 2-methyl-2-thio-, sulfate; Carbamimidothioic acid, methyl ester, sulfate (1:1) (9CI); 2-Methyl-2-thiopseudourea monosulfate; 2-Methylisothiouronium sulfate; Methyl thiopseudourea sulfate; S-Methylisothiourea sulfate (1:1); S-Methylpseudothiourea sulfate; S-Methylthiourea sulfate; S-Methylthiuronium sulfate; 2-Methylisothiouronium hydrogen sulphate; Carbamimidothioic acid, methyl ester, sulfate (1:1); Pseudourea, 2-methyl-2-thio-, hydrogen sulfate; Pseudourea, 2-methyl-2-thio-, sulfate (1:1) (8CI); methyl carbamimidothioate sulfate (2:1); (amino-methylsulfanyl-methylene)ammonium sulfate
• CAS NO: 147895-43-0
• Molecular Formula: C2H8N2O4S2
• Molecular Weight: 188.22592
• EINECS: 238-544-8
• Mol File: 147895-43-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 407°C at 760 mmHg
• Flash Point: 200°C
• Appearance: /
• Vapor Pressure: 9.15E-08mmHg at 25°C
• CAS DataBase Reference: CarbaMiMidothioic acid, Methyl ester, sulfate(CAS DataBase Reference)
• NIST Chemistry Reference: CarbaMiMidothioic acid, Methyl ester, sulfate(147895-43-0)
• EPA Substance Registry System: CarbaMiMidothioic acid, Methyl ester, sulfate(147895-43-0)

Safety Data

• Hazardous Substances Data: 147895-43-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C2H6N2S.H2O4S/c1-5-2(3)4;1-5(2,3)4/h1H3,(H3,3,4);(H2,1,2,3,4)/p-1

Upstream product

• 17356-08-0 thiourea 
• 77-78-1 dimethyl sulfate 
• 67-56-1 methanol 
• 37622-16-5 thiouronium hydrogensulfate 

Downstream Products

• 223687-91-0 1-(4-methylbenzoyl)-S-methylisothiourea 
• 46337-74-0 (4-isopropyl-benzyl)-guanidine 
• 162101-10-2 N-(4-chloro-phenylthiocarbamoyl)-S-methyl-isothiourea 
• 70104-51-7 (amino-methylsulfanyl-methylen)-amidophosphoric acid diphenyl ester 
• 47072-16-2 (o-Tolyl)-bis-(2-guanidino-ethyl)-amin 
• 75141-35-4 N-{4-[N',N''-Bis-(4-guanidino-butyl)-guanidino]-butyl}-benzamide 
• 46465-08-1 3-Benzylamino-propylguanidin 
• 18240-93-2 1,1-diethylguanidine 
• 29096-66-0 γ-<2,6-Dichlorphenyl>-propylaminoguanidin 
• 17187-55-2 5-(4-Hydroxybenzyl)-4-methylpyrimidin-2,6-diol 
• 50693-82-8 monoethylguanidine sulphate 
• 110893-75-9 N-(2-Hydroxy-3-o-tolylamino-propyl)-guanidine 
• 62936-50-9 N-(2-Hydroxy-3-phenylamino-propyl)-guanidine 
• 110893-82-8 N-(2-Hydroxy-3-p-tolylamino-propyl)-guanidine 

Relevant articles and documents

Thermal behavior and nucleation kinetics of 1,5-dimethyl-2-nitroimino-1, 3, 5-triazinane crystal

Nitroguanidine derivatives have increasingly gained attention because of their high insecticidal activities and wide spectrum. In this paper, nitroguanidine derivative 1,5-dimethyl-2-nitroimino-1, 3, 5-triazinane was synthesized, and its crystal structure was determined by X-ray technique. The thermal behaviors of 1, 5-dimethyl-2-nitroimino-1, 3, 5-triazinane in a nitrogen atmosphere were also studied under non-isothermal conditions by thermogravimetry (TG) and differential scanning calorimetry (DSC) techniques. The TG and DSC studies showed that the sample started to melt at 408.1 K with high melting enthalpy of 121.3 J/g and was stable up to at least 423.2 K, which indicated that the sample could be effectively utilized for various devices below 423.2 K. The melting entropy of 1,5-dimethyl-2-nitroimino-1, 3, 5-triazinane calculated from melting point and melting enthalpy using Eq. (1) was 51.476 J mol-1 K-1. In addition, the nucleation parameters of 1,5-dimethyl-2-nitroimino-1, 3, 5-triazinane in ethanol, such as the radius of critical nucleus and the Gibbs free energy barrier, had also been investigated based on classical nucleation theory. Crown Copyright

IMIDAZOPYRIMIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER

A compound of Formula (IA), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein A, R3, R4, R6, and R7 are as defined herein.

Tert -Butyl Hypochlorite Mediated Oxidative Chlorination of S -Alkylisothiourea Salts: Synthesis of Sulfonyl Chlorides

Under neutral conditions, a variety of S-alkylisothiourea salts were smoothly converted into the corresponding sulfonyl chlorides through tert-butyl chlorite mediated oxidative chlorination in good to excellent yields after simple purification. In addition to the environmental and procedural advantages of this method, the neutral conditions potentially make it applicable to substrates that bear acid-sensitive functional groups. For example, the Cbz-protected 2-aminoethanesulfonyl chloride could be synthesized in moderate to good yields under the current neutral conditions, and the acid-sensitive Cbz-protecting group was not affected.