Fenchlorazole-ethyl

Base Information

Chemical Name:Fenchlorazole-ethyl
CAS No.:103112-35-2
Molecular Formula:C12H8Cl5N3O2
Molecular Weight:403.479
Hs Code.:29339900
European Community (EC) Number:600-392-9,923-474-9
UNII:4R856T003A
DSSTox Substance ID:DTXSID6041268
Nikkaji Number:J474.548E
Wikidata:Q27155674
Metabolomics Workbench ID:127430
ChEMBL ID:CHEMBL2229892
Mol file:103112-35-2.mol

Synonyms:fenchlorazole-ethyl

Suppliers and Price of Fenchlorazole-ethyl

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
Fenchlorazol-ethyl
250mg
$ 375.00

TRC
Fenchlorazol-ethyl
100mg
$ 185.00

Sigma-Aldrich
Fenchlorazol-ethyl PESTANAL
50mg
$ 70.90

Total 35 raw suppliers

Chemical Property of Fenchlorazole-ethyl

Chemical Property:

Vapor Pressure:5.35E-09mmHg at 25°C
Melting Point:110 °C
Refractive Index:1.645
Boiling Point:469.8 °C at 760 mmHg
PKA:-3.59±0.50(Predicted)
Flash Point:237.9 °C
PSA：57.01000
Density:1.65 g/cm³
LogP:4.57750
XLogP3:5.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:402.902965
Heavy Atom Count:22
Complexity:409

Purity/Quality:

99% ^*data from raw suppliers

Fenchlorazol-ethyl ^*data from reagent suppliers

Safty Information:

Pictogram(s): T,N
Hazard Codes:T,N
Statements: 45-50/53
Safety Statements: 53-45-60-61

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl

Technology Process of Fenchlorazole-ethyl

There total 1 articles about Fenchlorazole-ethyl 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:

: 103112-35-2
ethyl 1-(2,4-dichloro-phenyl)-5trichloromethyl-1H-[1,2,4]triazole-3-carboxylate

Guidance literature:

Reference yield: 87.4%

: 103112-35-2
ethyl 1-(2,4-dichloro-phenyl)-5trichloromethyl-1H-[1,2,4]triazole-3-carboxylate

: 103112-36-3
1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; water; at 25 ℃; for 5h;

Reference yield:

: 103112-35-2
ethyl 1-(2,4-dichloro-phenyl)-5trichloromethyl-1H-[1,2,4]triazole-3-carboxylate

: 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carbonyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide / ethanol; water / 5 h / 25 °C

1.2: pH 1

2.1: thionyl chloride / dichloromethane / 1 h / 40 °C

With thionyl chloride; sodium hydroxide; In ethanol; dichloromethane; water;
DOI:10.3390/biom9090438