21722-13-4

Basic information

• Product Name: 4-fluorophenyl S-methylthiourea hydroiodide salt
• Synonyms: 4-fluorophenyl S-methylthiourea hydroiodide salt
• CAS NO: 21722-13-4
• Molecular Weight: 312.15
• Mol File: 21722-13-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-fluorophenyl S-methylthiourea hydroiodide salt(CAS DataBase Reference)
• NIST Chemistry Reference: 4-fluorophenyl S-methylthiourea hydroiodide salt(21722-13-4)
• EPA Substance Registry System: 4-fluorophenyl S-methylthiourea hydroiodide salt(21722-13-4)

Safety Data

• Hazardous Substances Data: 21722-13-4(Hazardous Substances Data)

Upstream product

• 459-05-2 (4-fluoro-phenyl)-thiourea 
• 74-88-4 methyl iodide 

Downstream Products

• 77391-30-1 N-(4-Fluoro-phenyl)-morpholine-4-carboxamidine; hydriodide 

Relevant articles and documents

Flavin receptors. Effect of the acidity of melamine derivatives bearing a 2-arylguanidinium ion on 6-azaflavin binding in chloroform

The pK(a)'s of melamine derivatives beating a 2-arylguanidinium ion and their binding constants for 6-aza-10dodecylisoalloxazine (6-azaflavin) were nicely correlated with the Hammett o of the substituents. However, the rates of the oxidations of N-benzyl-

PYRIMIDINDIONE DERIVATIVES AS PROKINETICIN 2 RECEPTOR ANTAGONISTS

The present invention relates to certain novel compounds of Formula (I), which are suitable for the treatment of prokineticin 2 or prokinetin 2 receptor mediated disorders.

Zur Kinetik der Oxydation 3-substituierter 1-Aminoguanidine durch Cerium(IV) in perchlorsaurer Loesung. 1. Teil

By known manners synthesized 1-amino-3-aryl-guanidines are oxidatively cyclized to corresponding 3,6-diarylamino-1,2,4,5-tetrazines in perchloric acid solution.The kinetics of this passing with second order model reaction was studied on a selected series of 17 1-amino-3-aryl-guanidine hydronitrates at 4 temperatures in 4 differently concentrated perchloric acid solutions of constant ionic strength by photometric concentration determination of oxidant cerium(IV).From experimental data rate constants, activation parameters and catalytic constants are evaluated by conventional methods, tabulated and discussed with regard to their substituent dependence.