144550-06-1

Basic information

• Product Name: methyl 4-iodo-2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate
• Synonyms: 144550-06-1; 429-890-2; iodosulfuron-methyl; T6N CN ENJ BO1 DMVMSWR CI FVO1& F1
• CAS NO: 144550-06-1
• Molecular Formula: C₁₄H₁₄IN₅O₆S
• Molecular Weight: 507.2603
• EINECS: 429-890-2
• Mol File: 144550-06-1.mol
• Article Data: 3

Chemical Properties

• Density: 1.806g/cm³
• Refractive Index: 1.636
• CAS DataBase Reference: methyl 4-iodo-2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 4-iodo-2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate(144550-06-1)
• EPA Substance Registry System: methyl 4-iodo-2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate(144550-06-1)

Safety Data

• Hazardous Substances Data: 144550-06-1(Hazardous Substances Data)

Upstream product

• 144550-77-6 (2-methoxycarbonyl-5-iodobenzene)disulfide 
• 144550-76-5 methyl 2-amino-4-iodobenzoate 
• 117324-10-4 2-acetylamino-4-iodobenzoic acid 
• 144550-79-8 2-methoxycarbonyl-5-iodobenzenesulfonamide 
• 102-09-0 bis(phenyl) carbonate 
• 1668-54-8 4-methoxy-6-methyl-1,3,5-triazin-2-amine 
• 144550-82-3 2-Methoxycarbonyl-5-iodobenzenesulfonyl isocyanate 

Downstream Products

• 144550-36-7 methyl 4-iodo-2-[[[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino] carbonyl]amino]sulfonyl]benzoate sodium salt 
• 208252-67-9 N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea 
• 1668-54-8 4-methoxy-6-methyl-1,3,5-triazin-2-amine 

Relevant articles and documents

PROCESS FOR PREPARING A NOVEL CRYSTALLINE FORM OF IODOSULFURON-METHYL-SODIUM AND USE OF THE SAME

A crystalline form of iodosulfuron-methyl-sodium of formula (I), the crystal preparation process, the analyses of the crystal through various analytical methods and using the crystal to prepare stable agrochemical formulation. The invention also describes the use of various solvents towards the crystalline form preparation conditions.

Process for the preparation of herbicidal sulfonylureas and of N-(pyrimidinyl or triazinyl)-carbamates as intermediate products

Disclosed and claimed is a process for the preparation of a carbamate (IV) by reaction of a salt with a diaryl carbonate The carbamate can be reacted, without any necessity of intermediate isolation, with a sulfonamide A--SO2 NH2 (V)