IPRODIONE

Base Information

• Chemical Name: IPRODIONE
• CAS No.: 63637-89-8
• Molecular Formula: C13H13 Cl2 N3 O3
• Molecular Weight: 330.171
• Hs Code.: 2934999090
• Mol file: 63637-89-8.mol

Synonyms:3-(1-Methylethyl)-N-(3,5-dichlorophenyl)-2,4-dioxo-1-imidazolidinecarboxamide;Isoiprodione; RP 30228

Chemical Property of IPRODIONE

Chemical Property:

• Melting Point: 130-134 °C(lit.)
• Boiling Point: °Cat760mmHg
• PKA: 10.47±0.70(Predicted)
• Flash Point: °C
• PSA: 69.72000
• Density: 1.511 g/cm³
• LogP: 3.14670

Purity/Quality:

99% ^*data from raw suppliers

Isoiprodione ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,N
• Hazard Codes: Xn,N
• Statements: 40-50/53
• Safety Statements: 36/37-60-61

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Isoiprodione is a constitutional isomer of Iprodione, a fungicide. Isoiprodione is a constitutional isomer of Iprodione (I745000), a fungicide.

Technology Process of IPRODIONE

There total 4 articles about IPRODIONE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

3-(isopropylcarbamoyl)-5-(3,5-dichlorophenyl)hydantoic acid (64952-42-7) → N-(3,5-dichlorophenyl)-3-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide (63637-89-8) + Iprodione (36734-19-7,61840-50-4)

Guidance literature:

In 1,4-dioxane; water; at 50 ℃; Rate constant; Mechanism; various buffers (pH range: 0.5 - 6);

DOI:10.1021/jo00278a037

Reference yield:

3-(isopropylcarbamoyl)-5-(3,5-dichlorophenyl)hydantoic acid (64952-42-7) → N-(3,5-dichlorophenyl)-3-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide (63637-89-8)

Guidance literature:

In ethanol; for 4h; Heating;

DOI:10.1021/jo00278a037

Reference yield:

Iprodione (36734-19-7,61840-50-4) → N-(3,5-dichlorophenyl)-3-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide (63637-89-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 1 M aq. NaOH / Ambient temperature

2: ethanol / 4 h / Heating

With sodium hydroxide; In ethanol;

DOI:10.1021/jo00278a037

upstream raw materials:

3-(isopropylcarbamoyl)-5-(3,5-dichlorophenyl)hydantoic acid

Iprodione

Refernces

• 1、 Belafdal, Omar,Bergon, Michel,Calmon, Michelle,Calmon, Jean Pierre. "Kinetics and Mechanisms of Cyclization in Acidic Media of N-N-glycine to Hydantoins: Iprodione and Its Isomer". . p. 4193 - 4198. Retrieved 2007/10/02.