ChemicalBook > Product Catalog >Chemical pesticides >Herbicide >Thiazafluron

Thiazafluron

Thiazafluron Suppliers list
Company Name: Suzhou Highfine Biotech Co., Ltd  
Tel: 0512-69209928 18796809688
Email: zhouyingxiang@highfine.com
Company Name: Shanghai Kewel Chemical Co., Ltd.  
Tel: 021-64609169 18901607656
Email: greensnown@163.com
Company Name: Hubei Yangxin Medical Technology Co., Ltd.  
Tel: 15374522761
Email: 3003392093@yongstandards.com
Company Name: Shenzhen Polymeri Biochemical Technology Co., Ltd.  
Tel: +86-400-002-6226
Email: sales@rrkchem.com
Company Name: Shanghai Jiegu Biotechnology Co., Ltd.  
Tel: 021-51698675
Email: sales@jiejiegroup.com
Thiazafluron Basic information
Product Name:Thiazafluron
Synonyms:2-(n,n’-dimethylureido)-5-trifluoromethyl-1,3,4-thiadiazole;4-thiadiazole,2-(n,n’-dimethylureido)-5-trifluoromethyl-3;erbotan;gs29296;n,n’-dimethyl-n-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)urea;1,3-DIMETHYL-1-(5-TRIFLUOROMETHYL-1,3,4-THIADIAZOL-2-YL)-UREA;thiazafluron (bsi,iso);thiazfluron (ISO) 1,3-dimethyl-1-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)urea
CAS:25366-23-8
MF:C6H7F3N4OS
MW:240.21
EINECS:246-901-4
Product Categories:Alpha sort;Herbicides;Pesticides&Metabolites;Q-ZAlphabetic;TF - TOPesticides&Metabolites;Urea structure
Mol File:25366-23-8.mol
Thiazafluron Structure
Thiazafluron Chemical Properties
Melting point 136.5°C
density 1.507±0.06 g/cm3(Predicted)
pka13.14±0.46(Predicted)
Water Solubility 2.096g/L(20 ºC)
BRN 806900
Henry's Law Constant3.2×104 mol/(m3Pa) at 25℃, MacBean (2012)
Safety Information
Hazard Codes Xn,N
Risk Statements 22-50/53
Safety Statements 60-61
RIDADR UN 2811 6.1/PG 3
WGK Germany 3
RTECS XI3760000
HS Code 29349990
Toxicitymouse,LD50,oral,630mg/kg (630mg/kg),"Agrochemicals Handbook," with updates, Hartley, D., and H. Kidd, eds., Nottingham, Royal Soc of Chemistry, 1983-86Vol. A392, Pg. 1983,
MSDS Information
Thiazafluron Usage And Synthesis
DefinitionChEBI: Thiazafluron is an organonitrogen heterocyclic compound and an organosulfur heterocyclic compound.
Production MethodsThiazafluron is produced commercially through a multi-step synthesis that constructs its substituted urea-thiadiazole structure. The process begins with the formation of a 1,3,4-thiadiazole ring, typically synthesised from thiosemicarbazide derivatives. This ring is then functionalised with a trifluoromethyl group to enhance herbicidal potency and environmental stability. The key intermediate is subsequently reacted with dimethylurea or its derivatives to form the final active compound, thiazafluron.
Mechanism of actionNon-selective, Photosynthetic electron transport inhibitor.
Pesticide TypeHerbicide
Thiazafluron Preparation Products And Raw materials
Tag:Thiazafluron(25366-23-8) Related Product Information
Aminoethoxyvinyl glycine hydrochloride Sulfometuron-methyl Prochloraz manganese 2-(Methylamino)-5-(trifluoromethyl)-1,3,4-thiadiazole Thiazafluron 2-Amino-5-trifluoromethyl-1,3,4-thiadiazole 2-Amino-1,3,4-thiadiazole 2-Amino-5-methyl-1,3,4-thiadiazole