Metconazole

Base Information

Chemical Name:Metconazole
CAS No.:125116-23-6
Molecular Formula:C17H22ClN3O
Molecular Weight:319.834
Hs Code.:
European Community (EC) Number:603-031-3
DSSTox Substance ID:DTXSID4034497
Nikkaji Number:J676.712E
Wikidata:Q1519339
ChEMBL ID:CHEMBL1883512
Mol file:125116-23-6.mol

Synonyms:(1S,5R)-5-((4-chlorophenyl)methyl)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol;5-((4-chlorophenyl)methyl)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol;cis-metconazole;metconazole

Suppliers and Price of Metconazole

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
Metconazole-d6
10mg
$ 1455.00

Sigma-Aldrich
Metconazole PESTANAL?, analytical standard, mixture of stereoisomers
100 mg
$ 106.00

Sigma-Aldrich
Metconazole mixture of isomers
100mg-r
$ 103.00

Medical Isotopes, Inc.
Metconazole
1 g
$ 975.00

American Custom Chemicals Corporation
METCONAZOLE 95.00%
250MG
$ 540.00

American Custom Chemicals Corporation
METCONAZOLE 95.00%
5MG
$ 402.80

AK Scientific
Metconazole
100mg
$ 85.00

AK Scientific
Metconazole
250mg
$ 187.00

Total 57 raw suppliers

Chemical Property of Metconazole

Chemical Property:

Vapor Pressure:1.33E-09mmHg at 25°C
Melting Point:111.5°C
Refractive Index:1.614
Boiling Point:469.1 °C at 760 mmHg
PKA:13.82±0.60(Predicted)
Flash Point:237.5 °C
PSA：50.94000
Density:1.24 g/cm³
LogP:3.34150
XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:319.1451400
Heavy Atom Count:22
Complexity:384

Purity/Quality:

98% ^*data from raw suppliers

Metconazole-d6 ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn; N
Hazard Codes:Xn,N
Statements: 22-51/53
Safety Statements: 60

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CCC(C1(CN2C=NC=N2)O)CC3=CC=C(C=C3)Cl)C
Uses Metconazole is an conazole based fungicide used for the control of black sigatoka disease on banana. Metconazole acts primarily as an inhibitor of ergosterol biosynthesis which interferes with the syn thesis of fungal cell membranes.

Technology Process of Metconazole

There total 29 articles about Metconazole 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: 91.6%

: C₁₅H₂₃ClN₂O

: 76085-56-8
N-(dichloromethyl)methanimidamide hydrochloride

: 125116-23-6
metconazole

Guidance literature:: In ethyl acetate; at 70 ℃; for 6h; Solvent; Temperature;

Reference yield: 85.0%

: 115851-28-0
5-[(4-chlorophenyl)methyl]-2,2-dimethylcyclopentanone

: 41253-21-8
sodium triazole

: 25596-24-1
trimethyloxosulfonium bromide

: 125116-23-6
metconazole

Guidance literature:: With sodium hydroxide; In 1-methyl-pyrrolidin-2-one; at 110 ℃; for 5h; Reagent/catalyst; Solvent; Temperature; Flow reactor; Inert atmosphere;