19932-87-7

Basic information

• Product Name: 2(3H)-BENZOXAZOLONE, 6-IODO-
• Synonyms: 2(3H)-BENZOXAZOLONE, 6-IODO-;6-Iodo-2,3-dihydro-1,3-benzoxazol-2-one
• CAS NO: 19932-87-7
• Molecular Formula: C₇H₄INO₂
• Molecular Weight: 261.01663
• Mol File: 19932-87-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2(3H)-BENZOXAZOLONE, 6-IODO-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(3H)-BENZOXAZOLONE, 6-IODO-(19932-87-7)
• EPA Substance Registry System: 2(3H)-BENZOXAZOLONE, 6-IODO-(19932-87-7)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 19932-87-7(Hazardous Substances Data)

Usage

General Description

2(3H)-Benzoxazolone, 6-Iodo- is a chemical compound with the molecular formula C7H5INO2. It is a derivative of benzoxazolone, which is a heterocyclic compound with a bicyclic structure. The presence of the iodo group in the molecule gives it unique properties and potential applications in various fields, such as organic synthesis, pharmaceuticals, and materials science. The compound may be used as a building block in the synthesis of other organic compounds or as a reagent in chemical reactions. Its specific uses and properties depend on the intended application and the reaction conditions in which it is used.

Upstream product

• 59-49-4 2-Benzoxazolinone 
• 16870-28-3 4-iodosalicylic acid 
• 603-87-2 2-amino-6-nitrophenol 
• 573-56-8 2,6-dinitrophenol 
• 28955-71-7 4-nitrobenzo[d]oxazol-2(3H)-one 
• 81900-93-8 4-amino-2-benzoxazolone 
• 606-21-3 1-chloro-2,6-dinitrobenzene 
• 19932-85-5 6-bromobenzo[d]oxazol-2(3H)-one 

Downstream Products

• 497084-49-8 6-iodo-8-quinolinol 
• 876346-93-9 C₁₁H₁₄INO₃ 

Relevant articles and documents

Method for synthesizing benzoxazole compound by using nitration by-products of aromatic hydrocarbon and application of benzoxazole compound

The invention discloses a method for synthesizing a benzoxazole compound by using nitration by-products of aromatic hydrocarbon and application of the benzoxazole compound. The method comprises the main process: performing step-by-step crystallization on nitration products of a 2,4-dinitrochlorobenzene production enterprise so as to obtain 2,4-dinitrochlorobenzene, 2,6-dinitrochlorobenzene (I) anda small amount of residues, adopting the obtained 2,6-dinitrochlorobenzene (I) as the main starting material, and performing hydrolysis, selective catalytic hydrogenation reduction, cyclization, halogenation, carbon-carbon coupling and other processes so as to synthesize the benzoxazole compound, wherein the obtained compound can be used as a main raw material to synthesize a series of chemical intermediates with important application, and the chemical intermediates include o-aminophenol, 2-amino-4-nitrophenol, 2-amino-5-nitrophenol and hydrochloride of o-aminophenol, 2-amino-4-nitrophenol, 2-amino-5-nitrophenol. Through the method, the industrial by-products are converted into high value-added aromatic aminophenol products, industrial hazardous waste of the 2,4-dinitrochlorobenzene production enterprise is reduced, the scope of products of the enterprise is widened, and the economic benefits of enterprise are increased.

HIV INHIBITING 1,2,4-TRIAZIN-6-ONE DERIVATIVES

The present invention relates to HIV replication inhibitors of formula (I) a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine or a stereochemically isomeric form thereof, wherein ring A and ring B represent phenyl, pyridyl, pyridaz

Preparation and antifungal activity of 3-Iodo- and 6-Iodo-8-quinolinols

3-Iodo- and 6-Iodo-8-quinolinols were prepared and tested against six fungi: Aspergillus niger, A. oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes in Sabouraud dextrose broth. A comparison with the previously known 5-iodo- and 7-iodo-8-quinolinols showed that the 6-iodo isomer was the most active.