854538-41-3

Usage

Molecular Weight

429.97 g/mol

Structure

A resorcinol derivative with two hydroxyl groups at the 1,3 positions, two iodine atoms at the 4,6 positions, and two acetate groups attached to the hydroxyl groups.

Appearance

Yellow to light brown crystalline solid

Solubility

Soluble in organic solvents like ethanol, methanol, and acetone

Uses

a. Organic synthesis
b. Reagent in chemical reactions
c. Pharmaceutical formulation
d. Potential applications in the medical field

Antimicrobial

Exhibits antimicrobial activity against certain microorganisms

Antioxidant

Demonstrates antioxidant properties, potentially useful in the development of antioxidant agents

Hazards

Can be hazardous if not handled properly; precautions should be taken during storage and use

Storage

Store in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames

Safety Measures

Use appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats when handling this chemical

Disposal

Dispose of in accordance with local, national, and international regulations for hazardous materials

Synonyms

4,6-Diiodo-resorcinol diacetate, 1,3-Benzenediol, 4,6-diiodo-diacetate, 4,6-Diiodoresorcinol diacetate

Chemical Classification

Aromatic compound, Halogenated hydrocarbon, Resorcinol derivative

Melting Point

Approximately 176-178°C (349-354°F)

Boiling Point

Not readily available, but expected to be high due to the presence of iodine atoms

Density

Not readily available, but expected to be higher than water due to the presence of iodine atoms

Stability

Stable under normal conditions, but sensitive to heat, light, and moisture

Reactivity

Reacts with strong oxidizing agents, strong acids, and strong bases

Regulatory Information

May be subject to specific regulations depending on the country and intended use (e.g., pharmaceutical, industrial, or research applications)

Upstream product

• 19514-91-1 4,6-diiodobenzene-1,3-diol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 925900-90-9 2,4-bis(hex-1'-ynyl)-1,5-diacetoxybenzene 
• 1002158-15-7 2,4-di(oct-1'-ynyl)-1,5-diacetoxybenzene 
• 925900-88-5 2,4-bis(3'-benzyloxyprop-1'-ynyl)-1,5-bis(pent-4'-enyloxy)benzene 
• 925900-87-4 1,5-bis(but-3'-enyloxy)-2,4-bis(3'-benzyloxyprop-1'-ynyl)benzene 
• 925900-86-3 1,5-bis(hex-1'-ynyl)-1,5-bis(pent-4'-enyloxy)benzene 
• 925900-80-7 1,5-bis(allyloxy)-2,4-bis(3'-benzyloxyprop-1'-ynyl)-benzene 
• 925900-85-2 1,5-bis(but-3'-enyloxy)-2,4-di(hex-1'-ynyl)benzene 
• 925900-78-3 1-allyloxy-5-(but-3'-enyloxy)-2,4-bis(hex-1'-ynyl)benzene 
• 925900-79-4 2,4-bis(3'-benzyloxyprop-1'-ynyl)-1,5-dihydroxybenzene 
• 925900-76-1 1,5-bis(allyloxy)-2,4-bis(hex-1'-ynyl)benzene 
• 925900-77-2 5-(but-3'-enyloxy)-2,4-bis(hex-1'-ynyl)phenol 
• 925900-75-0 2,4-bis(hex-1'-ynyl)-1,5-dihydroxybenzene 
• 1002158-14-6 2,4-bis(tert-butylethynyl)-1,5-diacetoxybenzene 

Relevant academic research and scientific papers

An efficient synthesis of fused tricycles with a benzene core via intramolecular double ring-closing enyne metathesis

A double enyne metathesis reaction has been developed for the efficient synthesis of tricyclic products with a benzene core in good yields. By this protocol, bisannulated benzenes with different ring sizes may be simultaneously constructed from the corres

Highly conductive poly(phenylene thienylene)s: M-phenylene linkages are not always bad

Two isomeric polymers, which contain meta- or para-phenylene linkages between conducting segments, have been synthesized and compared by electrochemical methods. The nonconjugated poly-(1,5-diacetoxy-m-phenylene tetrathienylene) (PMPT-OAc) showed similar