Cismethrin

Base Information

Chemical Name:Cismethrin
CAS No.:35764-59-1
Deprecated CAS:31182-61-3
Molecular Formula:C₂₂H₂₆O₃
Molecular Weight:338.447
Hs Code.:
UNII:2VWB5PVB6A
UN Number:3349
DSSTox Substance ID:DTXSID9091525,DTXSID7091547
ICSC Number:0239
Metabolomics Workbench ID:144225
Nikkaji Number:J20.251G
Wikidata:Q864681
Mol file:35764-59-1.mol

Synonyms:5-benzyl-3-furylmethyl(1.R)-cis-chrysanthemate;cismethrin;cismethrin, 14C-labeled, (1R-cis)-isomer;cismethrin, cis-(+-)-isomer;cismethrin, cis-(-)-isomer;NRDC 119

Suppliers and Price of Cismethrin

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

Total 6 raw suppliers

Chemical Property of Cismethrin

Chemical Property:

Vapor Pressure:4.07E-07mmHg at 25°C
Melting Point:45 °C
Refractive Index:1.5000 (estimate)
Boiling Point:415.6°Cat760mmHg
Flash Point:205.2°C
PSA：39.44000
Density:1.111g/cm³
LogP:4.90340
XLogP3:6.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:338.18819469
Heavy Atom Count:25
Complexity:497

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=CC1C(C1(C)C)C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C
Isomeric SMILES:CC(=C[C@H]1[C@H](C1(C)C)C(=O)OCC2=COC(=C2)CC3=CC=CC=C3)C
Inhalation Risk:Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly on spraying or when dispersed, especially if powdered.
Effects of Short Term Exposure:The substance is mildly irritating to the eyes and skin. The substance may cause effects on the nervous system.

Technology Process of Cismethrin

There total 4 articles about Cismethrin 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: 92.0%

: 20416-09-5
(5-benzylfuran-3-yl)methanol

: 10453-86-8,10453-55-1,35764-59-1,33911-28-3
resmethrin

Guidance literature:

Reference yield:

: 39856-63-8
2-benzyl-4-methyl-oxazole

: 10453-86-8,10453-55-1,35764-59-1,33911-28-3
resmethrin

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent Turnov_. / hydroquinone / 2 h / 220 °C

2: 82 percent Turnov_. / 5percent-natriumethanolate / toluene / 4 h / Heating

With sodium ethanolate; hydroquinone; In toluene;

Reference yield:

: 627-09-8
Propargyl acetate

: 10453-86-8,10453-55-1,35764-59-1,33911-28-3
resmethrin

Guidance literature:: Multi-step reaction with 2 steps

1: 58 percent Turnov_. / hydroquinone / 2 h / 220 °C

2: 82 percent Turnov_. / 5percent-natriumethanolate / toluene / 4 h / Heating

With sodium ethanolate; hydroquinone; In toluene;