135773-25-0

Basic information

• Product Name: N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE
• Synonyms: N,N-Dimethyl 4-iodo-1H-imidazole-;1-(Dimethylsulfamoyl)-4-iodo-1H-imidazole;N,N-Dimethyl-4-iodo-1H-imidazol-1-sulfonamide;4-Iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide;N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE;N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULPHONAMIDE;N,N-DIMENTHYL-4-IODO-1H-IMIDAZOLE-1SULFONA
• CAS NO: 135773-25-0
• Molecular Formula: C₅H₈IN₃O₂S
• Molecular Weight: 301.11
• Product Categories: Imidazoles;Iodides;Sulfonamides;blocks
• Mol File: 135773-25-0.mol
• Article Data: 8

Chemical Properties

• Melting Point: 119-122°C
• Boiling Point: 387.275 °C at 760 mmHg
• Flash Point: 188.017 °C
• Appearance: /
• Density: 2.049 g/cm³
• Vapor Pressure: 3.33E-06mmHg at 25°C
• Refractive Index: 1.687
• Storage Temp.: Keep Cold
• PKA: -0.04±0.61(Predicted)
• CAS DataBase Reference: N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE(135773-25-0)
• EPA Substance Registry System: N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE(135773-25-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 135773-25-0(Hazardous Substances Data)

Usage

General Description

N,N-Dimethyl 4-Iodo-1H-Imidazole-1-sulfonamide is a chemical compound with the molecular formula C6H8N4O2S. It is a sulfonamide derivative with a substituted imidazole ring, and it contains a dimethyl amine group. N,N-DIMETHYL 4-IODO-1H-IMIDAZOLE-1-SULFONAMIDE is commonly used in pharmaceutical research and drug development as it exhibits antibacterial and antifungal properties. It is also used as a reagent in organic synthesis and in the preparation of various bioactive molecules. Furthermore, N,N-Dimethyl 4-Iodo-1H-Imidazole-1-sulfonamide is an important intermediate in the synthesis of potential biologically active compounds.

InChI:InChI=1/C5H8IN3O2S/c1-8(2)12(10,11)9-3-5(6)7-4-9/h3-4H,1-2H3

Upstream product

• 3034-62-6 2-iodo-1H-imidazole 
• 71759-89-2 4-iodoimidazole 
• 13360-57-1 dimethylamino sulfonyl chloride 
• 198127-92-3 4,5-diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide 

Downstream Products

• 135799-03-0 4-(Hydroxy-phenyl-methyl)-imidazole-1-sulfonic acid dimethylamide 
• 725233-26-1 4-(3-nitrophenylsulfanyl)imidazole-1-sulfonic acid dimethylamide 
• 1449431-53-1 C₂₃H₃₀N₆O₅S 
• 1449431-47-3 methyl 4-(1-(benzyloxy)-3-(1-(N,N-dimethylsulfamoyl)-1H-imidazole-4-yl)-1H-pyrazol-4-yl)piperidine-1-carboxylate 
• 1269422-70-9 N-(3-(1-(N,N-dimethylsulfamoyl)-1H-imidazol-4-yl)prop-2-ynyl)-N-trityl-1H-pyrrole-2-carboxamide 
• 1269422-75-4 N-(3-(1-(N,N-dimethylsulfamoyl)-1H-imidazol-4-yl)prop-2-ynyl)-1-methyl-N-trityl-1H-pyrrole-2-carboxamide 
• 1258289-23-4 4,4'-[3-(dibenzylamino)-1-hydroxypropane-1,1-diyl]bis(N,N-dimethyl-1H-imidazole-1-sulfonamide) 
• 1029690-49-0 4-(3-bromobenzyl)imidazole-1-sulfonic acid dimethylamide 
• 258527-71-8 1H-imidazol-4-yl(4-methoxy-3-nitrophenyl)methanol 
• 699021-08-4 4-(4-pyridinylmethyl)imidazole-1-sulfonic acid dimethylamide 
• 725233-28-3 4-(3-ethanesulfonylaminophenylsulfanyl)imidazole-1-sulfonic acid dimethylamide 
• 258528-03-9 N,N-dimethyl-4-[1-(3-nitrophenyl)vinyl]-1H-imidazole-1-sulfonamide 
• 725233-27-2 4-(3-aminophenylsulfanyl)imidazole-1-sulfonic acid dimethylamide 
• 258528-04-0 4-[1-(3-aminophenyl)ethyl]-N,N-dimethyl-1H-imidazole-1-sulfonamide 

Relevant articles and documents

Characterization of the binding site of the histamine H3 receptor. 1. Various approaches to the synthesis of 2-(1H-imidazol-4-yl)cyclopropylamine and histaminergic activity of (1R,2R)- and (1S,2S)-2-(1H-imidazol-4-yl)- cyclopropylamine

Various approaches to the synthesis of all four stereoisomers of 2-(1H- imidazol-4-yl)cyclopropylamine (cyclopropylhistamine) are described. The rapid and convenient synthesis and resolution of trans-cyclopropylhistamine is reported. The absolute configur

Total synthesis of the putative structure of nagelamide D

A total synthesis of the putative structure of nagelamide D from imidazole is described. A Stille cross-coupling is used to construct the bis imidazole skeleton, and the pyrrolecarboxamides are introduced via a double Mitsunobu reaction using a pyrrolehyd

Certain Nitrogen Containing Bicyclic Chemical Entities for Treating Viral Infections

Provided are certain chemical entities, pharmaceutical compositions, and methods of treatment of a member of the flaviviradae family of viruses such as hepacivirus (Hepatitis C or HCV).