Mandipropamid

Base Information

Chemical Name:Mandipropamid
CAS No.:374726-62-2
Deprecated CAS:1135441-79-0
Molecular Formula:C23H22ClNO4
Molecular Weight:411.885
Hs Code.:
UNII:11GP4ELK0U
ChEMBL ID:CHEMBL271907
DSSTox Substance ID:DTXSID4058075
Nikkaji Number:J2.290.045E
Wikidata:Q2057167
Mol file:374726-62-2.mol

Synonyms:2-(4-chlorophenyl)-N-(2-(3-methoxy-4-(2-propyn-1-yloxy)phenyl)ethyl)-2-(2-propyn-1-yloxy)acetamide;mandipropamid;MPD fungicide

Suppliers and Price of Mandipropamid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Mandipropamid
10mg
$ 120.00

Sigma-Aldrich
Mandipropamid PESTANAL?, analytical standard
100mg
$ 139.00

Medical Isotopes, Inc.
Mandipropamid
2.5 g
$ 2600.00

Medical Isotopes, Inc.
Mandipropamid
100 mg
$ 610.00

Total 0 raw suppliers

Chemical Property of Mandipropamid

Chemical Property:

Vapor Pressure:9.38E-15mmHg at 25°C
Melting Point:96-97 °C
Refractive Index:1.574
Boiling Point:608.6 °C at 760 mmHg
PKA:13.90±0.46(Predicted)
Flash Point:321.8 °C
PSA：60.28000
Density:1.214g/cm³
LogP:4.25070
Storage Temp.:Hygroscopic, -20°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), Dichloromethane (Slightly)
XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:411.1237359
Heavy Atom Count:29
Complexity:599

Purity/Quality:: Mandipropamid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=CC(=C1)CCNC(=O)C(C2=CC=C(C=C2)Cl)OCC#C)OCC#C
Uses Mandipropamid is a fungicide. It can be used on many fruit and vegetable crops, including potatoes, tomatoes, salad leaves and grapes. Manufactured by Syngenta.

Technology Process of Mandipropamid

There total 3 articles about Mandipropamid 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: 79.0%

: 282720-26-7
2-(4-chlorophenyl)-2-hydroxy-N-[2-(3-methoxy-4-(prop-2-ynyloxy)phenyl)ethyl]acetamide

: 106-96-7
propargyl bromide

: 374726-62-2
mandipropamid

Guidance literature:: With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; water; toluene; at 40 ℃; for 16h;
DOI:10.1016/j.bmc.2007.10.019