372136-76-0

Basic information

• Product Name: SulfaMide, N-Methyl-N-(1-Methylethyl)-
• Synonyms: SulfaMide, N-Methyl-N-(1-Methylethyl)-;N-isopropyl-N-methylsulfamide;N-Methyl-N-isopropylsulfamoyl amide;N-methyl-N-(1-methylethyl)aminosulfonamide
• CAS NO: 372136-76-0
• Molecular Formula: C₄H₁₂N₂O₂S
• Molecular Weight: 152.215
• Mol File: 372136-76-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: Acetone; Dichloromethane; Methanol
• CAS DataBase Reference: SulfaMide, N-Methyl-N-(1-Methylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: SulfaMide, N-Methyl-N-(1-Methylethyl)-(372136-76-0)
• EPA Substance Registry System: SulfaMide, N-Methyl-N-(1-Methylethyl)-(372136-76-0)

Safety Data

• Hazardous Substances Data: 372136-76-0(Hazardous Substances Data)

Usage

Uses

N-Isopropyl-N-methylsulfamide is an intermediate in the synthesis of unlabeled Saflufenacil-d7 (S081802). Saflufenacil-d7 is the labeled version of Saflufenacil (S081800), which is a herbicide of the pyrimidinedione chemical class used for the preplant burndown and selective preemergence dicot weed control in different field crops. It was found to inhibit protoporphyrinogen IX oxidase (PPO) enzyme.

Upstream product

• 263169-13-7 N-isopropyl-N-methyl-sulphamoyl chloride 
• 958002-25-0 tert-butyl N-isopropyl-N-methylsulfamoylcarbamate 

Downstream Products

• 1033905-10-0 C₃₂H₃₉N₃O₆S 
• 940005-46-9 N-(2-chloro-4-fluoro-3-nitrobenzoyl)-N'-isopropyl-N'-methylsulfamide 
• 940005-45-8 N-(4-fluoro-3-nitrobenzoyl)-N'-isopropyl-N'-methylsulfamide 
• 372137-35-4 saflufenacil 

Relevant articles and documents

Methods for Producing Sulfonic Acid Diamides

The present invention relates to a process for preparing sulfuric diamides of the general formula I [in-line-formulae]R1R2N—S(O)2—NH2??(I)[/in-line-formulae] in which R1 and R2 are each ind

CYCLOPROPYL FUSED INDOLOBENZAZEPINE HCV NS5B INHIBITORS

The invention encompasses compounds of formula (I) as well as compositions and methods of using the compounds. The compounds have activity against hepatitis C virus (HCV) and are useful in treating those infected with HCV

Uracil substituted phenyl sulfamoyl carboxamides

Novel uracil substituted phenyl sulfamoyl carboxamides I and salts thereof, where A=oxygen or sulfur; X1=H, halogen, C1-C4-alkyl; X2=H, CN, CS—NH2, halogen, C1-C4-alkyl, C1-C4-haloalkyl; X3=H, CN, C1-C6-alkyl, C1-C6-alkoxyalkyl, C3-C7-cycloalkyl, C3-C6-alkenyl, C3-C6-alkynyl, optionally substituted benzyl; R1, R2=H, halogen, optionally substituted hydroxy, C1-C10-alkyl, C2-C10-alkenyl, C3-C10-alkynyl, C3-C7-cycloalkyl, phenyl, benzyl or C5-C7-cycloalkenyl, or R1+R2 together with the atom to which they are attached form a 3- to 7-membered heterocyclic ring; Q is selected from Q1 to Q40 as defined in the description. Use: As herbicides; for the desiccation/defoliation of plants.