Cyprodinil

Base Information

• Chemical Name: Cyprodinil
• CAS No.: 121552-61-2
• Molecular Formula: C14H15N3
• Molecular Weight: 225.293
• Hs Code.: 2942000000
• European Community (EC) Number: 601-785-8
• UNII: 42P6T6OFWZ
• DSSTox Substance ID: DTXSID1032359
• Nikkaji Number: J682.437D
• Wikidata: Q3008902
• Metabolomics Workbench ID: 46715
• ChEMBL ID: CHEMBL521027
• Mol file: 121552-61-2.mol

Synonyms:cyprodinil

Chemical Property of Cyprodinil

Chemical Property:

• Appearance/Colour: off-white solid
• Vapor Pressure: 8.42E-07mmHg at 25°C
• Melting Point: 75.9 °C
• Refractive Index: 1.659
• Boiling Point: 405.985 °C at 760 mmHg
• PKA: 4.44 (base)
• Flash Point: 199.333 °C
• PSA: 37.81000
• Density: 1.21 g/cm³
• LogP: 3.47900
• Storage Temp.: 0-6°C
• Water Solubility.: 20 mg l-1 (pH 5), 13 mg l-1 (pH 7), 15 mg l-1 (pH 9) 25 °C
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 225.126597491
• Heavy Atom Count: 17
• Complexity: 246

Purity/Quality:

99% ^*data from raw suppliers

Cyprodinil ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/38-43
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Pesticides -> Fungicides
• Canonical SMILES: CC1=CC(=NC(=N1)NC2=CC=CC=C2)C3CC3
• Uses: Cyprodinil is a broad-spectrum fungicide of the class of pyrimidinamines. It is commonly used for protection of cereal crops and fruits against fungal infections. Agricultural fungicide. Cyprodinil is a systemic fungicide which controls a wide range of fungal diseases in cereals, grapes, pome fruits, stone fruits, berries, vegetables, field crops and ornamentals caused by Septoria, Botrytis, Monilinia, Rhynchosporium, etc.

Technology Process of Cyprodinil

There total 2 articles about Cyprodinil 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: 74.5%

1-cyclopropyl-butane-1,3-dione (21573-10-4) + phenylguanidinium hydrogencarbonate (6685-76-3) → 4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine (121552-61-2)

Guidance literature:

In diethyl ether; water;

Reference yield:

→ 4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine (121552-61-2)

Guidance literature:

Reference yield: 36.5%

4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine (121552-61-2) → 4-(4-Cyclopropyl-6-methyl-pyrimidin-2-ylamino)-phenol + 4-Cyclopropyl-2-(4-hydroxy-phenylamino)-6-methyl-pyrimidin-5-ol

Guidance literature:

With Absidia pseudocylindraspora; In ethanol;

DOI:10.1021/jf970298l

upstream raw materials:

1-cyclopropyl-butane-1,3-dione

phenylguanidinium hydrogencarbonate

Downstream raw materials:

2-Amino-4-cyclopropyl-6-methyl-pyrimidine

cyprodinil 2-aminopyrimidine co-crystal

cyprodinil ethyl maltol co-crystal

cyprodinil succinamide co-crystal