826-97-1

Usage

General Description

2,4,6-Tribromophenyl isocyanate 97 is a chemical compound with the molecular formula C6H3Br3NO. It is a highly reactive compound used in the production of flame retardants and other materials. It is capable of forming strong bonds with other materials, and is often used in the production of polyurethane foams, adhesives, and coatings. Due to its reactivity and potential health hazards, it must be handled with extreme care and in accordance with proper safety protocols. Additionally, its use is regulated in many industries to minimize its potential environmental and health impacts.

InChI:InChI=1/C7H2Br3NO/c8-4-1-5(9)7(11-3-12)6(10)2-4/h1-2H

Upstream product

• 75-44-5 phosgene 
• 50522-41-3 2,4,6-tribromo-aniline; hydrochloride 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 147-82-0 2,4,6-tribromoaniline 
• 201230-82-2 carbon monoxide 
• 3463-40-9 2,4,6-tribromonitrobenzene 

Downstream Products

• 50602-68-1 N,N'-bis-(2,4,6-tribromo-phenyl)-urea 
• 16289-37-5 3-(2,4,6-tribromophenyl)-2,4(1H,3H)-quinazolinedione 
• 89892-46-6 2-chloro-N-(2,4,6-tribromophenyl)acetamide 

Relevant academic research and scientific papers

Specific inhibitors of puromycin-sensitive aminopeptidase with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton

Specific puromycin-sensitive aminopeptidase (PSA) inhibitors with a 3-(halogenated phenyl)-2,4(1H,3H)-quinazolinedione skeleton were prepared and their structure-activity relationships were investigated. The nature (F, Cl or Br), number and position(s) of the halogen atom(s) introduced into the 3-phenyl group were concluded to be critical determinants of the inhibitory activity.

Synthesis of new substituted 6-ureidopurines and 6-ureido-9-(2,3,5-triacetyl ribofuranosyl)purines having cytokinin (plant growth promoting) activity

Substituted 6-ureidopurines 6a-j and 6-ureido-9-(2,3,5-triacetylribofuranosyl) purines 7a-j have been synthesized by condensing substituted phenyl isocyanates with adenine 3 and 2,3,5-triacetyladenosine 5 respectively in pyridine. Substituted phenyl isocyanates 2a-j are prepared from substituted anilines 1a-j in the presence of triphosgene and triethylamine in dry benzene. Compounds 6a-j and 7a-j have been evaluated for cytokinin activity on seeds of Raphanus sativus, family Brassicaceae (common name white radish) at 5 different concentrations in distilled water ranging from 0.001 to 10 mg litre-1. Compounds 6a, 7a, 7b and 7i having substitutents at 3 position of phenyl ring are found to show higher cytokinin activity than benzyladenine at all concentrations (Table II).