tolonidine

tolonidine Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:Tolonidine
CAS:4201-22-3
Package:10 mg;2 mg;5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: CR Corporation Lomited
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Email: fred.wen@crcorporation.cn
Products Intro: Product Name:tolonidine
CAS:4201-22-3
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
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Products Intro: Product Name:Tolonidine
CAS:4201-22-3
Purity:99% Package:5mg;10mg;25mg
Company Name: Beijing Solarbio Science & Tecnology Co., Ltd.  
Tel: 010-50973130 4009686088
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Products Intro: CAS:4201-22-3
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:Tolonidine
CAS:4201-22-3
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
tolonidine Basic information
Product Name:tolonidine
Synonyms:tolonidine;N-(2-Chloro-4-methylphenyl)-4,5-dihydro-1H-imidazol-2-amine;ST-375;1H-Imidazol-2-amine, N-(2-chloro-4-methylphenyl)-4,5-dihydro-
CAS:4201-22-3
MF:C10H12ClN3
MW:209.68
EINECS:
Product Categories:
Mol File:4201-22-3.mol
tolonidine Structure
tolonidine Chemical Properties
Melting point 148-150°
Boiling point 314.0±52.0 °C(Predicted)
density 1.31±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka9.41(at 25℃)
Safety Information
MSDS Information
tolonidine Usage And Synthesis
OriginatorEuctan,Essex,Switz.,1978
DefinitionChEBI: Tolonidine is a substituted aniline.
Manufacturing Process43 g of the thiourea compound (melting point 124°C) obtained in known fashion from 2-chloro-4-methylaniline and ammonium thiocyanate and 20 cc of methyl iodide were dissolved in 200 cc of methanol, and the solution was refluxed for two hours.1 Thereafter, the solvent was evaporated in vacuo, leaving 73.2 g of the isothiouronium hydroiodide of the formula as a residue. This isothiouronium salt was admixed with 20 cc of ethylenediamine, and the mixture was heated for about 30 minutes at 150°C to 160°C, accompanied by stirring; methyl mercaptan escaped during that time. Subsequently, the reaction mixture was taken up in hot dilute acetic acid, and the resulting solution was made alkaline with 2 N sodium hydroxide. A precipitate formed, which was separated by vacuum filtration, washed with water and dried. It was identified to be 2-(2'-chloro-4'-methylphenyl)-amino-1,3- diazacyclopentene-(2) having a melting point of 142°C to 145°C. The yield was 10.2 g.
The nitrate of the base, obtained by acidifying a solution of the free base with nitric acid, had a melting point of 162°C to 164°C and was soluble in water and methanol.
Therapeutic FunctionAntihypertensive
tolonidine Preparation Products And Raw materials
Raw materialsEthylenediamine-->Nitric acid-->2-Chloro-4-methylaniline-->Iodomethane-->Ammonium thiocyanate
Tag:tolonidine(4201-22-3) Related Product Information
N-(2-CHLORO-PHENYL)-GUANIDINE N-P-TOLYL-GUANIDINE HYDROCHLORIDE N-P-TOLYL-GUANIDINE Benzamide, 5-chloro-N-(2-(diethylamino)ethyl)-4-((4,5-dihydro-1H-imida zol-2-yl)amino)-2-methoxy- tolonidine CHLOROETHYLCLONIDINE